dbVar data for all organisms

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Variant Placements (including Supporting Variants) for nstd143
Study ID	Variant ID	Variant Region type	Variant Call type	Sampleset ID	Method	Analysis ID	Validation	Assembly	Accession	Chr	Start	End	Placement Type	Remap Score
nstd143	nssv14038729		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000011.9	11	5217204	5285011	Submitted genomic
nstd143	nssv14038729		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000011.9	11	5217204	5285011	Submitted genomic
nstd143	nssv14038729		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh38.p12	NC_000011.10	11	5195974	5263781	Remapped	1
nstd143	nssv14038730		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000011.9	11	5135464	5254173	Submitted genomic
nstd143	nssv14038730		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000011.9	11	5135464	5254173	Submitted genomic
nstd143	nssv14038730		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh38.p12	NC_000011.10	11	5114234	5232943	Remapped	1
nstd143	nssv14038731		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000011.9	11	5157109	5361649	Submitted genomic
nstd143	nssv14038731		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000011.9	11	5157109	5361649	Submitted genomic
nstd143	nssv14038731		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh38.p12	NC_000011.10	11	5135879	5340419	Remapped	1
nstd143	nssv14038732		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000011.9	11	5247824	5255222	Submitted genomic
nstd143	nssv14038732		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000011.9	11	5247824	5255222	Submitted genomic
nstd143	nssv14038732		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh38.p12	NC_000011.10	11	5226594	5233992	Remapped	1
nstd143	nssv14038733		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	71955	235250	Submitted genomic
nstd143	nssv14038733		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	71955	235250	Submitted genomic
nstd143	nssv14038733		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh38.p12	NC_000016.10	16	21955	185251	Remapped	1.00001
nstd143	nssv14038734		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	84105	238055	Submitted genomic
nstd143	nssv14038734		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	84105	238055	Submitted genomic
nstd143	nssv14038734		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh38.p12	NC_000016.10	16	34105	188056	Remapped	1.00001
nstd143	nssv14038735		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	123895	245125	Submitted genomic
nstd143	nssv14038735		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	123895	245125	Submitted genomic
nstd143	nssv14038735		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh38.p12	NC_000016.10	16	73897	195126	Remapped	0.99999
nstd143	nssv14038736		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	155381	290220	Submitted genomic
nstd143	nssv14038736		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	155381	290220	Submitted genomic
nstd143	nssv14038736		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh38.p12	NC_000016.10	16	105383	240221	Remapped	0.99999
nstd143	nssv14038737		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	196190	258010	Submitted genomic
nstd143	nssv14038737		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	196190	258010	Submitted genomic
nstd143	nssv14038737		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh38.p12	NC_000016.10	16	146191	208011	Remapped	1
nstd143	nssv14038738		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	208663	235974	Submitted genomic
nstd143	nssv14038738		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	208663	235974	Submitted genomic
nstd143	nssv14038738		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh38.p12	NC_000016.10	16	158664	185975	Remapped	1
nstd143	nssv14038739		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	215125	284579	Submitted genomic
nstd143	nssv14038739		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	215125	284579	Submitted genomic
nstd143	nssv14038739		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh38.p12	NC_000016.10	16	165126	234580	Remapped	1
nstd143	nssv14038740		complex substitution	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	94455	281325	Submitted genomic
nstd143	nssv14038740		complex substitution	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	94455	281325	Submitted genomic
nstd143	nssv14038740		complex substitution	1	Sequencing	Read depth and paired-end mapping	No	GRCh38.p12	NC_000016.10	16	44455	231326	Remapped	1.00001
nstd143	nssv14038741		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	97115	175257	Submitted genomic
nstd143	nssv14038741		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	97115	175257	Submitted genomic
nstd143	nssv14038741		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh38.p12	NC_000016.10	16	47115	125258	Remapped	1.00001
nstd143	nssv14038742		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	97615	299525	Submitted genomic
nstd143	nssv14038742		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	97615	299525	Submitted genomic
nstd143	nssv14038742		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh38.p12	NC_000016.10	16	47615	249526	Remapped	1
nstd143	nssv14038743		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	215144	236065	Submitted genomic
nstd143	nssv14038743		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	215144	236065	Submitted genomic
nstd143	nssv14038743		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh38.p12	NC_000016.10	16	165145	186066	Remapped	1
nstd143	nssv14038744		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	221260	252033	Submitted genomic
nstd143	nssv14038744		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	221260	252033	Submitted genomic
nstd143	nssv14038744		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh38.p12	NC_000016.10	16	171261	202034	Remapped	1
nstd143	nssv14038745		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	222201	227178	Submitted genomic
nstd143	nssv14038745		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	222201	227178	Submitted genomic
nstd143	nssv14038745		duplication	1	Sequencing	Read depth and paired-end mapping	No	GRCh38.p12	NC_000016.10	16	172202	177179	Remapped	1
nstd143	nssv14038746		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	227121	228400	Submitted genomic
nstd143	nssv14038746		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh37 (hg19)	NC_000016.9	16	227121	228400	Submitted genomic
nstd143	nssv14038746		deletion	1	Sequencing	Read depth and paired-end mapping	No	GRCh38.p12	NC_000016.10	16	177122	178401	Remapped	1
nstd143	nsv3067123	copy number variation					No	GRCh37 (hg19)	NC_000016.9	16	222201	227178	Submitted genomic
nstd143	nsv3067123	copy number variation					No	GRCh37 (hg19)	NC_000016.9	16	222201	227178	Submitted genomic
nstd143	nsv3067123	copy number variation					No	GRCh38.p12	NC_000016.10	16	172202	177179	Remapped	1
nstd143	nsv3067124	copy number variation					No	GRCh37 (hg19)	NC_000016.9	16	227121	228400	Submitted genomic
nstd143	nsv3067124	copy number variation					No	GRCh37 (hg19)	NC_000016.9	16	227121	228400	Submitted genomic
nstd143	nsv3067124	copy number variation					No	GRCh38.p12	NC_000016.10	16	177122	178401	Remapped	1
nstd143	nsv3067125	copy number variation					No	GRCh37 (hg19)	NC_000016.9	16	123895	245125	Submitted genomic
nstd143	nsv3067125	copy number variation					No	GRCh37 (hg19)	NC_000016.9	16	123895	245125	Submitted genomic
nstd143	nsv3067125	copy number variation					No	GRCh38.p12	NC_000016.10	16	73897	195126	Remapped	0.99999
nstd143	nsv3067126	copy number variation					No	GRCh37 (hg19)	NC_000016.9	16	155381	290220	Submitted genomic
nstd143	nsv3067126	copy number variation					No	GRCh37 (hg19)	NC_000016.9	16	155381	290220	Submitted genomic
nstd143	nsv3067126	copy number variation					No	GRCh38.p12	NC_000016.10	16	105383	240221	Remapped	0.99999
nstd143	nsv3067127	complex substitution					No	GRCh37 (hg19)	NC_000016.9	16	94455	281325	Submitted genomic
nstd143	nsv3067127	complex substitution					No	GRCh37 (hg19)	NC_000016.9	16	94455	281325	Submitted genomic
nstd143	nsv3067127	complex substitution					No	GRCh38.p12	NC_000016.10	16	44455	231326	Remapped	1.00001
nstd143	nsv3067128	copy number variation					No	GRCh37 (hg19)	NC_000016.9	16	97115	175257	Submitted genomic
nstd143	nsv3067128	copy number variation					No	GRCh37 (hg19)	NC_000016.9	16	97115	175257	Submitted genomic
nstd143	nsv3067128	copy number variation					No	GRCh38.p12	NC_000016.10	16	47115	125258	Remapped	1.00001
nstd143	nsv3067129	copy number variation					No	GRCh37 (hg19)	NC_000011.9	11	5217204	5285011	Submitted genomic
nstd143	nsv3067129	copy number variation					No	GRCh37 (hg19)	NC_000011.9	11	5217204	5285011	Submitted genomic
nstd143	nsv3067129	copy number variation					No	GRCh38.p12	NC_000011.10	11	5195974	5263781	Remapped	1
nstd143	nsv3067130	copy number variation					No	GRCh37 (hg19)	NC_000016.9	16	196190	258010	Submitted genomic
nstd143	nsv3067130	copy number variation					No	GRCh37 (hg19)	NC_000016.9	16	196190	258010	Submitted genomic
nstd143	nsv3067130	copy number variation					No	GRCh38.p12	NC_000016.10	16	146191	208011	Remapped	1
nstd143	nsv3067131	copy number variation					No	GRCh37 (hg19)	NC_000011.9	11	5135464	5254173	Submitted genomic
nstd143	nsv3067131	copy number variation					No	GRCh37 (hg19)	NC_000011.9	11	5135464	5254173	Submitted genomic
nstd143	nsv3067131	copy number variation					No	GRCh38.p12	NC_000011.10	11	5114234	5232943	Remapped	1
nstd143	nsv3067132	copy number variation					No	GRCh37 (hg19)	NC_000011.9	11	5157109	5361649	Submitted genomic
nstd143	nsv3067132	copy number variation					No	GRCh37 (hg19)	NC_000011.9	11	5157109	5361649	Submitted genomic
nstd143	nsv3067132	copy number variation					No	GRCh38.p12	NC_000011.10	11	5135879	5340419	Remapped	1
nstd143	nsv3067133	copy number variation					No	GRCh37 (hg19)	NC_000011.9	11	5247824	5255222	Submitted genomic
nstd143	nsv3067133	copy number variation					No	GRCh37 (hg19)	NC_000011.9	11	5247824	5255222	Submitted genomic
nstd143	nsv3067133	copy number variation					No	GRCh38.p12	NC_000011.10	11	5226594	5233992	Remapped	1
nstd143	nsv3067134	copy number variation					No	GRCh37 (hg19)	NC_000016.9	16	71955	235250	Submitted genomic
nstd143	nsv3067134	copy number variation					No	GRCh37 (hg19)	NC_000016.9	16	71955	235250	Submitted genomic
nstd143	nsv3067134	copy number variation					No	GRCh38.p12	NC_000016.10	16	21955	185251	Remapped	1.00001
nstd143	nsv3067135	copy number variation					No	GRCh37 (hg19)	NC_000016.9	16	84105	238055	Submitted genomic
nstd143	nsv3067135	copy number variation					No	GRCh37 (hg19)	NC_000016.9	16	84105	238055	Submitted genomic
nstd143	nsv3067135	copy number variation					No	GRCh38.p12	NC_000016.10	16	34105	188056	Remapped	1.00001
nstd143	nsv3067136	copy number variation					No	GRCh37 (hg19)	NC_000016.9	16	97615	299525	Submitted genomic
nstd143	nsv3067136	copy number variation					No	GRCh37 (hg19)	NC_000016.9	16	97615	299525	Submitted genomic
nstd143	nsv3067136	copy number variation					No	GRCh38.p12	NC_000016.10	16	47615	249526	Remapped	1
nstd143	nsv3067137	copy number variation					No	GRCh37 (hg19)	NC_000016.9	16	208663	235974	Submitted genomic
nstd143	nsv3067137	copy number variation					No	GRCh37 (hg19)	NC_000016.9	16	208663	235974	Submitted genomic
nstd143	nsv3067137	copy number variation					No	GRCh38.p12	NC_000016.10	16	158664	185975	Remapped	1
nstd143	nsv3067138	copy number variation					No	GRCh37 (hg19)	NC_000016.9	16	215125	284579	Submitted genomic

dbVar

Database of genomic structural variation

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