dbVar data for all organisms

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Variant Placements (including Supporting Variants) for nstd213 (displaying 100 of 11800 variants)
Study ID	Variant ID	Variant Region type	Variant Call type	Method	Analysis ID	Validation	Variant samples	Assembly	Accession	Chr	Outer-Start	Start	Inner-Start	Inner-End	End	Outer-End	Placement Type	Remap Score
nstd213	nssv17677376		intrachromosomal translocation	Sequencing	Paired-end mapping	No	LNCaP_C42b	GRCh38.p12	NC_000001.11	1		11368983			11368983		Remapped	1
nstd213	nssv17677376		intrachromosomal translocation	Sequencing	Paired-end mapping	No	LNCaP_C42b	GRCh38.p12	NC_000001.11	1		8367752			8367752		Remapped	1
nstd213	nssv17677762		copy number gain	Sequencing	Paired-end mapping	No	LAPC4-CR	GRCh38.p12	NC_000001.11	1		5499940			5759941		Remapped	1
nstd213	nssv17677792		intrachromosomal translocation	Sequencing	Paired-end mapping	No	LNCaP	GRCh38.p12	NC_000001.11	1		11372414			11372414		Remapped	1
nstd213	nssv17678033		copy number loss	Sequencing	Paired-end mapping	No	DU145	GRCh38.p12	NC_000001.11	1		7199940			8249941		Remapped	1
nstd213	nssv17678446		copy number loss	Sequencing	Paired-end mapping	No	PC3	GRCh38.p12	NC_000001.11	1		9219941			9469942		Remapped	1
nstd213	nssv17678449		copy number gain	Sequencing	Paired-end mapping	No	VCaP	GRCh38.p12	NC_000001.11	1		5829940			5969941		Remapped	1
nstd213	nssv17678588		copy number loss	Sequencing	Paired-end mapping	No	PC3	GRCh38.p12	NC_000001.11	1		10749943			10839944		Remapped	1
nstd213	nssv17678613		copy number loss	Sequencing	Paired-end mapping	No	LNCaP	GRCh38.p12	NC_000001.11	1		14743504			16563506		Remapped	1
nstd213	nssv17678671		copy number gain	Sequencing	Paired-end mapping	No	LAPC4	GRCh38.p12	NC_000001.11	1		6899940			7069941		Remapped	1
nstd213	nssv17678763		copy number loss	Sequencing	Paired-end mapping	No	PC3	GRCh38.p12	NC_000001.11	1		6969940			7119941		Remapped	1
nstd213	nssv17678920		copy number loss	Sequencing	Paired-end mapping	No	LNCaP_C42b	GRCh38.p12	NC_000001.11	1		14743504			16503506		Remapped	1
nstd213	nssv17679123		copy number loss	Sequencing	Paired-end mapping	No	DU145	GRCh38.p12	NC_000001.11	1		8369940			11579944		Remapped	1
nstd213	nssv17679145		intrachromosomal translocation	Sequencing	Paired-end mapping	No	LNCaP_Abl	GRCh38.p12	NC_000001.11	1		11372388			11372388		Remapped	1
nstd213	nssv17679181		copy number loss	Sequencing	Paired-end mapping	No	PC3	GRCh38.p12	NC_000001.11	1		8319940			8409941		Remapped	1
nstd213	nssv17679743		copy number loss	Sequencing	Paired-end mapping	No	DU145	GRCh38.p12	NC_000001.11	1		784620			1644640		Remapped	1.00002
nstd213	nssv17679871		copy number loss	Sequencing	Paired-end mapping	No	PC3	GRCh38.p12	NC_000001.11	1		7259940			7359941		Remapped	1
nstd213	nssv17680080		copy number gain	Sequencing	Paired-end mapping	No	LAPC4-CR	GRCh38.p12	NC_000001.11	1		7189940			7289941		Remapped	1
nstd213	nssv17680256		intrachromosomal translocation	Sequencing	Paired-end mapping	No	LNCaP_C42b	GRCh38.p12	NC_000001.11	1		11372402			11372402		Remapped	1
nstd213	nssv17680290		copy number gain	Sequencing	Paired-end mapping	No	LAPC4-CR	GRCh38.p12	NC_000001.11	1		7699940			7799941		Remapped	1
nstd213	nssv17680307		copy number loss	Sequencing	Paired-end mapping	No	PC3	GRCh38.p12	NC_000001.11	1		11529943			11589944		Remapped	1
nstd213	nssv17680472		copy number loss	Sequencing	Paired-end mapping	No	DU145	GRCh38.p12	NC_000001.11	1		2773454			3173437		Remapped	0.99996
nstd213	nssv17680613		copy number loss	Sequencing	Paired-end mapping	No	PC3	GRCh38.p12	NC_000001.11	1		13633505			13893506		Remapped	1
nstd213	nssv17680777		duplication	Sequencing	Paired-end mapping	No	LNCaP_C42b	GRCh38.p12	NC_000001.11	1	8774169		8774171	9094662		9094664	Remapped	1
nstd213	nssv17680993		copy number gain	Sequencing	Paired-end mapping	No	LAPC4-CR	GRCh38.p12	NC_000001.11	1		3723436			3883437		Remapped	1
nstd213	nssv17681371		copy number loss	Sequencing	Paired-end mapping	No	LNCaP_Abl	GRCh38.p12	NC_000001.11	1		14743504			16563506		Remapped	1
nstd213	nssv17681425		intrachromosomal translocation	Sequencing	Paired-end mapping	No	LNCaP_Abl	GRCh38.p12	NC_000001.11	1		8403779			8403779		Remapped	1
nstd213	nssv17681425		intrachromosomal translocation	Sequencing	Paired-end mapping	No	LNCaP_Abl	GRCh38.p12	NC_000001.11	1		9696844			9696844		Remapped	1
nstd213	nssv17681467		intrachromosomal translocation	Sequencing	Paired-end mapping	No	LNCaP_Abl	GRCh38.p12	NC_000001.11	1		10713844			10713844		Remapped	1
nstd213	nssv17681467		intrachromosomal translocation	Sequencing	Paired-end mapping	No	LNCaP_Abl	GRCh38.p12	NC_000001.11	1		14744298			14744298		Remapped	1
nstd213	nssv17681490		copy number loss	Sequencing	Paired-end mapping	No	DU145	GRCh38.p12	NC_000001.11	1		6239940			6949941		Remapped	1
nstd213	nssv17681502		copy number loss	Sequencing	Paired-end mapping	No	DU145	GRCh38.p12	NC_000001.11	1		4409940			4869941		Remapped	1
nstd213	nssv17681596		copy number gain	Sequencing	Paired-end mapping	No	LNCaP_C42b	GRCh38.p12	NC_000001.11	1		8859941			9039942		Remapped	1
nstd213	nssv17681624		intrachromosomal translocation	Sequencing	Paired-end mapping	No	LNCaP_Abl	GRCh38.p12	NC_000001.11	1		12108243			12108243		Remapped	1
nstd213	nssv17681624		intrachromosomal translocation	Sequencing	Paired-end mapping	No	LNCaP_Abl	GRCh38.p12	NC_000001.11	1		9694561			9694561		Remapped	1
nstd213	nssv17681670		copy number loss	Sequencing	Paired-end mapping	No	DU145	GRCh38.p12	NC_000001.11	1		1748561			1958562		Remapped	1
nstd213	nssv17681733		copy number loss	Sequencing	Paired-end mapping	No	DU145	GRCh38.p12	NC_000001.11	1		3939940			4219941		Remapped	1
nstd213	nssv17681962		intrachromosomal translocation	Sequencing	Paired-end mapping	No	LNCaP	GRCh38.p12	NC_000001.11	1		8403758			8403758		Remapped	1
nstd213	nssv17681962		intrachromosomal translocation	Sequencing	Paired-end mapping	No	LNCaP	GRCh38.p12	NC_000001.11	1		9696858			9696858		Remapped	1
nstd213	nssv17682029		copy number loss	Sequencing	Paired-end mapping	No	PC3	GRCh38.p12	NC_000001.11	1		10979943			11089944		Remapped	1
nstd213	nssv17682185		intrachromosomal translocation	Sequencing	Paired-end mapping	No	LNCaP_C42b	GRCh38.p12	NC_000001.11	1		10713824			10713824		Remapped	1
nstd213	nssv17682185		intrachromosomal translocation	Sequencing	Paired-end mapping	No	LNCaP_C42b	GRCh38.p12	NC_000001.11	1		14744301			14744301		Remapped	1
nstd213	nssv17682462		copy number loss	Sequencing	Paired-end mapping	No	PC3	GRCh38.p12	NC_000001.11	1		8579941			8749942		Remapped	1
nstd213	nssv17682900		copy number loss	Sequencing	Paired-end mapping	No	DU145	GRCh38.p12	NC_000001.11	1		14983504			15523506		Remapped	1
nstd213	nssv17682936		copy number loss	Sequencing	Paired-end mapping	No	DU145	GRCh38.p12	NC_000001.11	1		13190972			13833506		Remapped	1.25987
nstd213	nssv17682941		intrachromosomal translocation	Sequencing	Paired-end mapping	No	LNCaP_Abl	GRCh38.p12	NC_000001.11	1		11368980			11368980		Remapped	1
nstd213	nssv17682941		intrachromosomal translocation	Sequencing	Paired-end mapping	No	LNCaP_Abl	GRCh38.p12	NC_000001.11	1		8367752			8367752		Remapped	1
nstd213	nssv17682990		copy number loss	Sequencing	Paired-end mapping	No	PC3	GRCh38.p12	NC_000001.11	1		14493504			14583505		Remapped	1
nstd213	nssv17683039		copy number loss	Sequencing	Paired-end mapping	No	PC3	GRCh38.p12	NC_000001.11	1		10169942			10239943		Remapped	1
nstd213	nssv17683333		copy number gain	Sequencing	Paired-end mapping	No	LAPC4-CR	GRCh38.p12	NC_000001.11	1		8219940			8319941		Remapped	1
nstd213	nsv6133421	copy number variation				No		GRCh38.p12	NC_000001.11	1		10169942			10239943		Remapped	1
nstd213	nsv6133493	copy number variation				No		GRCh38.p12	NC_000001.11	1		10749943			10839944		Remapped	1
nstd213	nsv6133497	copy number variation				No		GRCh38.p12	NC_000001.11	1		13190972			13833506		Remapped	1.25987
nstd213	nsv6133498	copy number variation				No		GRCh38.p12	NC_000001.11	1		13633505			13893506		Remapped	1
nstd213	nsv6133553	copy number variation				No		GRCh38.p12	NC_000001.11	1		14743504			16503506		Remapped	1
nstd213	nsv6133558	copy number variation				No		GRCh38.p12	NC_000001.11	1		14983504			15523506		Remapped	1
nstd213	nsv6133589	copy number variation				No		GRCh38.p12	NC_000001.11	1		15773505			15983506		Remapped	1
nstd213	nsv6133657	copy number variation				No		GRCh38.p12	NC_000001.11	1		6239940			6949941		Remapped	1
nstd213	nsv6133660	copy number variation				No		GRCh38.p12	NC_000001.11	1		784620			1644640		Remapped	1.00002
nstd213	nsv6133662	copy number variation				No		GRCh38.p12	NC_000001.11	1		7699940			7799941		Remapped	1
nstd213	nsv6133665	copy number variation				No		GRCh38.p12	NC_000001.11	1		8319940			8409941		Remapped	1
nstd213	nsv6133668	copy number variation				No		GRCh38.p12	NC_000001.11	1		8859941			9039942		Remapped	1
nstd213	nsv6133721	copy number variation				No		GRCh38.p12	NC_000001.11	1	8774169		8774171	9094662		9094664	Remapped	1
nstd213	nsv6133727	copy number variation				No		GRCh38.p12	NC_000001.11	1		10979943			11089944		Remapped	1
nstd213	nsv6133731	copy number variation				No		GRCh38.p12	NC_000001.11	1		14493504			14583505		Remapped	1
nstd213	nsv6133745	copy number variation				No		GRCh38.p12	NC_000001.11	1		1748561			1958562		Remapped	1
nstd213	nsv6133770	copy number variation				No		GRCh38.p12	NC_000001.11	1		2773454			3173437		Remapped	0.99996
nstd213	nsv6133776	copy number variation				No		GRCh38.p12	NC_000001.11	1		5499940			5759941		Remapped	1
nstd213	nsv6133779	copy number variation				No		GRCh38.p12	NC_000001.11	1		6969940			7119941		Remapped	1
nstd213	nsv6133780	copy number variation				No		GRCh38.p12	NC_000001.11	1		7189940			7289941		Remapped	1
nstd213	nsv6133781	copy number variation				No		GRCh38.p12	NC_000001.11	1		7259940			7359941		Remapped	1
nstd213	nsv6133782	copy number variation				No		GRCh38.p12	NC_000001.11	1		9219941			9469942		Remapped	1
nstd213	nsv6133875	copy number variation				No		GRCh38.p12	NC_000001.11	1		5829940			5969941		Remapped	1
nstd213	nsv6133876	copy number variation				No		GRCh38.p12	NC_000001.11	1		6899940			7069941		Remapped	1
nstd213	nsv6133877	copy number variation				No		GRCh38.p12	NC_000001.11	1		7199940			8249941		Remapped	1
nstd213	nsv6133884	copy number variation				No		GRCh38.p12	NC_000001.11	1		8369940			11579944		Remapped	1
nstd213	nsv6133885	copy number variation				No		GRCh38.p12	NC_000001.11	1		8579941			8749942		Remapped	1
nstd213	nsv6133920	copy number variation				No		GRCh38.p12	NC_000001.11	1		11529943			11589944		Remapped	1
nstd213	nsv6133923	copy number variation				No		GRCh38.p12	NC_000001.11	1		14743504			16563506		Remapped	1
nstd213	nsv6133993	copy number variation				No		GRCh38.p12	NC_000001.11	1		3723436			3883437		Remapped	1
nstd213	nsv6133995	copy number variation				No		GRCh38.p12	NC_000001.11	1		3939940			4219941		Remapped	1
nstd213	nsv6133996	copy number variation				No		GRCh38.p12	NC_000001.11	1		4409940			4869941		Remapped	1
nstd213	nsv6134250	copy number variation				No		GRCh38.p12	NC_000001.11	1		8219940			8319941		Remapped	1
nstd213	nsv6136422	translocation				No		GRCh38.p12	NC_000001.11	1		8403758			8403758		Remapped	1
nstd213	nsv6136422	translocation				No		GRCh38.p12	NC_000001.11	1		9696858			9696858		Remapped	1
nstd213	nsv6136424	translocation				No		GRCh38.p12	NC_000001.11	1		10713844			10713844		Remapped	1
nstd213	nsv6136424	translocation				No		GRCh38.p12	NC_000001.11	1		14744298			14744298		Remapped	1
nstd213	nsv6136427	translocation				No		GRCh38.p12	NC_000001.11	1		11368980			11368980		Remapped	1
nstd213	nsv6136427	translocation				No		GRCh38.p12	NC_000001.11	1		8367752			8367752		Remapped	1
nstd213	nsv6136430	translocation				No		GRCh38.p12	NC_000001.11	1		10713824			10713824		Remapped	1
nstd213	nsv6136430	translocation				No		GRCh38.p12	NC_000001.11	1		14744301			14744301		Remapped	1
nstd213	nsv6136432	translocation				No		GRCh38.p12	NC_000001.11	1		11372402			11372402		Remapped	1
nstd213	nsv6137123	translocation				No		GRCh38.p12	NC_000001.11	1		11372414			11372414		Remapped	1
nstd213	nsv6137127	translocation				No		GRCh38.p12	NC_000001.11	1		8403779			8403779		Remapped	1
nstd213	nsv6137127	translocation				No		GRCh38.p12	NC_000001.11	1		9696844			9696844		Remapped	1
nstd213	nsv6137491	translocation				No		GRCh38.p12	NC_000001.11	1		12108243			12108243		Remapped	1
nstd213	nsv6137491	translocation				No		GRCh38.p12	NC_000001.11	1		9694561			9694561		Remapped	1
nstd213	nsv6137493	translocation				No		GRCh38.p12	NC_000001.11	1		11372388			11372388		Remapped	1
nstd213	nsv6137501	translocation				No		GRCh38.p12	NC_000001.11	1		11368983			11368983		Remapped	1
nstd213	nsv6137501	translocation				No		GRCh38.p12	NC_000001.11	1		8367752			8367752		Remapped	1

dbVar

Database of genomic structural variation

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