dbVar data for all organisms

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Variant Placements (including Supporting Variants) for nstd164
Study ID	Variant ID	Variant Region type	Variant Call type	Method	Analysis ID	Validation	Variant samples	Assembly	Accession	Chr	Outer-Start	Inner-Start	Inner-End	Outer-End	Placement Type	Remap Score
nstd164	nssv14814876		copy number loss	Oligo aCGH	Curated	No	P006	GRCh37 (hg19)	NC_000017.10	17	58089454	58090137	60346028	60346711	Submitted genomic
nstd164	nssv14814876		copy number loss	Oligo aCGH	Curated	No	P006	GRCh37 (hg19)	NC_000017.10	17	58089454	58090137	60346028	60346711	Submitted genomic
nstd164	nssv14814876		copy number loss	Oligo aCGH	Curated	No	P006	GRCh38.p12	NC_000017.11	17	60012093	60012776	62268667	62269350	Remapped	1
nstd164	nssv14814877		copy number loss	Oligo aCGH	Curated	No	P009	GRCh37 (hg19)	NC_000017.10	17	58090283	58090656	60346857	60347230	Submitted genomic
nstd164	nssv14814877		copy number loss	Oligo aCGH	Curated	No	P009	GRCh37 (hg19)	NC_000017.10	17	58090283	58090656	60346857	60347230	Submitted genomic
nstd164	nssv14814877		copy number loss	Oligo aCGH	Curated	No	P009	GRCh38.p12	NC_000017.11	17	60012922	60013295	62269496	62269869	Remapped	1
nstd164	nssv14814878		copy number loss	Oligo aCGH	Curated	No	P012	GRCh37 (hg19)	NC_000017.10	17	58088933	58089453	60345508	60346028	Submitted genomic
nstd164	nssv14814878		copy number loss	Oligo aCGH	Curated	No	P012	GRCh37 (hg19)	NC_000017.10	17	58088933	58089453	60345508	60346028	Submitted genomic
nstd164	nssv14814878		copy number loss	Oligo aCGH	Curated	No	P012	GRCh38.p12	NC_000017.11	17	60011572	60012092	62268147	62268667	Remapped	1
nstd164	nssv14814879		copy number loss	Oligo aCGH	Curated	No	P019	GRCh37 (hg19)	NC_000017.10	17		58167485	60174066		Submitted genomic
nstd164	nssv14814879		copy number loss	Oligo aCGH	Curated	No	P019	GRCh37 (hg19)	NC_000017.10	17		58167485	60174066		Submitted genomic
nstd164	nssv14814879		copy number loss	Oligo aCGH	Curated	No	P019	GRCh38.p12	NC_000017.11	17		60090124	62096705		Remapped	1
nstd164	nssv14814880		copy number loss	Oligo aCGH	Curated	No	P026	GRCh37 (hg19)	NC_000017.10	17	58088933	58089453	60345508	60346028	Submitted genomic
nstd164	nssv14814880		copy number loss	Oligo aCGH	Curated	No	P026	GRCh37 (hg19)	NC_000017.10	17	58088933	58089453	60345508	60346028	Submitted genomic
nstd164	nssv14814880		copy number loss	Oligo aCGH	Curated	No	P026	GRCh38.p12	NC_000017.11	17	60011572	60012092	62268147	62268667	Remapped	1
nstd164	nssv14814881		copy number loss	Oligo aCGH	Curated	No	P073	GRCh37 (hg19)	NC_000017.10	17	58086876	58087936	60343456	60344516	Submitted genomic
nstd164	nssv14814881		copy number loss	Oligo aCGH	Curated	No	P073	GRCh37 (hg19)	NC_000017.10	17	58086876	58087936	60343456	60344516	Submitted genomic
nstd164	nssv14814881		copy number loss	Oligo aCGH	Curated	No	P073	GRCh38.p12	NC_000017.11	17	60009515	60010575	62266095	62267155	Remapped	1
nstd164	nssv14814882		copy number loss	Oligo aCGH	Curated	No	P035	GRCh37 (hg19)	NC_000017.10	17	59272842	59272846	61392993	61392997	Submitted genomic
nstd164	nssv14814882		copy number loss	Oligo aCGH	Curated	No	P035	GRCh37 (hg19)	NC_000017.10	17	59272842	59272846	61392993	61392997	Submitted genomic
nstd164	nssv14814882		copy number loss	Oligo aCGH	Curated	No	P035	GRCh38.p12	NC_000017.11	17	61195481	61195485	63315632	63315636	Remapped	1
nstd164	nssv14814883		copy number loss	Oligo aCGH	Curated	No	P015	GRCh37 (hg19)	NC_000017.10	17	59542891	59542894	59551500	59551503	Submitted genomic
nstd164	nssv14814883		copy number loss	Oligo aCGH	Curated	No	P015	GRCh37 (hg19)	NC_000017.10	17	59542891	59542894	59551500	59551503	Submitted genomic
nstd164	nssv14814883		copy number loss	Oligo aCGH	Curated	No	P015	GRCh38.p12	NC_000017.11	17	61465530	61465533	61474139	61474142	Remapped	1
nstd164	nssv14814884		copy number loss	Oligo aCGH	Curated	No	P016	GRCh37 (hg19)	NC_000017.10	17	59542891	59542894	59551500	59551503	Submitted genomic
nstd164	nssv14814884		copy number loss	Oligo aCGH	Curated	No	P016	GRCh37 (hg19)	NC_000017.10	17	59542891	59542894	59551500	59551503	Submitted genomic
nstd164	nssv14814884		copy number loss	Oligo aCGH	Curated	No	P016	GRCh38.p12	NC_000017.11	17	61465530	61465533	61474139	61474142	Remapped	1
nstd164	nssv14814885		copy number loss	Oligo aCGH	Curated	No	P038	GRCh37 (hg19)	NC_000017.10	17	58857889	58857898	58868328	58868337	Submitted genomic
nstd164	nssv14814885		copy number loss	Oligo aCGH	Curated	No	P038	GRCh37 (hg19)	NC_000017.10	17	58857889	58857898	58868328	58868337	Submitted genomic
nstd164	nssv14814885		copy number loss	Oligo aCGH	Curated	No	P038	GRCh38.p12	NC_000017.11	17	60780528	60780537	60790967	60790976	Remapped	1
nstd164	nssv14814886		copy number loss	Sequencing	Curated	No	P040	GRCh37 (hg19)	NC_000005.9	5	43957152	43957220	46135141	46135209	Submitted genomic
nstd164	nssv14814886		copy number loss	Sequencing	Curated	No	P040	GRCh37 (hg19)	NC_000005.9	5	43957152	43957220	46135141	46135209	Submitted genomic
nstd164	nssv14814886		copy number loss	Sequencing	Curated	No	P040	GRCh38.p12	NC_000005.10	5	43957050	43957118	46135039	46135107	Remapped	1
nstd164	nssv14814887		copy number loss	Sequencing	Curated	No	P041	GRCh37 (hg19)	NC_000005.9	5	43957152	43957220	46135141	46135209	Submitted genomic
nstd164	nssv14814887		copy number loss	Sequencing	Curated	No	P041	GRCh37 (hg19)	NC_000005.9	5	43957152	43957220	46135141	46135209	Submitted genomic
nstd164	nssv14814887		copy number loss	Sequencing	Curated	No	P041	GRCh38.p12	NC_000005.10	5	43957050	43957118	46135039	46135107	Remapped	1
nstd164	nssv14814888		copy number loss	Sequencing	Curated	No	P076	GRCh37 (hg19)	NC_000005.9	5		42985023	45244787		Submitted genomic
nstd164	nssv14814888		copy number loss	Sequencing	Curated	No	P076	GRCh37 (hg19)	NC_000005.9	5		42985023	45244787		Submitted genomic
nstd164	nssv14814888		copy number loss	Sequencing	Curated	No	P076	GRCh38.p12	NC_000005.10	5		42984921	45244685		Remapped	1
nstd164	nsv3418821	copy number variation				No		GRCh37 (hg19)	NC_000005.9	5	43957152	43957220	46135141	46135209	Submitted genomic
nstd164	nsv3418821	copy number variation				No		GRCh37 (hg19)	NC_000005.9	5	43957152	43957220	46135141	46135209	Submitted genomic
nstd164	nsv3418821	copy number variation				No		GRCh38.p12	NC_000005.10	5	43957050	43957118	46135039	46135107	Remapped	1
nstd164	nsv3418822	copy number variation				No		GRCh37 (hg19)	NC_000017.10	17	58088933	58089453	60345508	60346028	Submitted genomic
nstd164	nsv3418822	copy number variation				No		GRCh37 (hg19)	NC_000017.10	17	58088933	58089453	60345508	60346028	Submitted genomic
nstd164	nsv3418822	copy number variation				No		GRCh38.p12	NC_000017.11	17	60011572	60012092	62268147	62268667	Remapped	1
nstd164	nsv3418823	copy number variation				No		GRCh37 (hg19)	NC_000017.10	17	59542891	59542894	59551500	59551503	Submitted genomic
nstd164	nsv3418823	copy number variation				No		GRCh37 (hg19)	NC_000017.10	17	59542891	59542894	59551500	59551503	Submitted genomic
nstd164	nsv3418823	copy number variation				No		GRCh38.p12	NC_000017.11	17	61465530	61465533	61474139	61474142	Remapped	1
nstd164	nsv3418824	copy number variation				No		GRCh37 (hg19)	NC_000005.9	5		42985023	45244787		Submitted genomic
nstd164	nsv3418824	copy number variation				No		GRCh37 (hg19)	NC_000005.9	5		42985023	45244787		Submitted genomic
nstd164	nsv3418824	copy number variation				No		GRCh38.p12	NC_000005.10	5		42984921	45244685		Remapped	1
nstd164	nsv3418825	copy number variation				No		GRCh37 (hg19)	NC_000017.10	17		58167485	60174066		Submitted genomic
nstd164	nsv3418825	copy number variation				No		GRCh37 (hg19)	NC_000017.10	17		58167485	60174066		Submitted genomic
nstd164	nsv3418825	copy number variation				No		GRCh38.p12	NC_000017.11	17		60090124	62096705		Remapped	1
nstd164	nsv3418826	copy number variation				No		GRCh37 (hg19)	NC_000017.10	17	58086876	58087936	60343456	60344516	Submitted genomic
nstd164	nsv3418826	copy number variation				No		GRCh37 (hg19)	NC_000017.10	17	58086876	58087936	60343456	60344516	Submitted genomic
nstd164	nsv3418826	copy number variation				No		GRCh38.p12	NC_000017.11	17	60009515	60010575	62266095	62267155	Remapped	1
nstd164	nsv3418827	copy number variation				No		GRCh37 (hg19)	NC_000017.10	17	58089454	58090137	60346028	60346711	Submitted genomic
nstd164	nsv3418827	copy number variation				No		GRCh37 (hg19)	NC_000017.10	17	58089454	58090137	60346028	60346711	Submitted genomic
nstd164	nsv3418827	copy number variation				No		GRCh38.p12	NC_000017.11	17	60012093	60012776	62268667	62269350	Remapped	1
nstd164	nsv3418828	copy number variation				No		GRCh37 (hg19)	NC_000017.10	17	58090283	58090656	60346857	60347230	Submitted genomic
nstd164	nsv3418828	copy number variation				No		GRCh37 (hg19)	NC_000017.10	17	58090283	58090656	60346857	60347230	Submitted genomic
nstd164	nsv3418828	copy number variation				No		GRCh38.p12	NC_000017.11	17	60012922	60013295	62269496	62269869	Remapped	1
nstd164	nsv3418829	copy number variation				No		GRCh37 (hg19)	NC_000017.10	17	58857889	58857898	58868328	58868337	Submitted genomic
nstd164	nsv3418829	copy number variation				No		GRCh37 (hg19)	NC_000017.10	17	58857889	58857898	58868328	58868337	Submitted genomic
nstd164	nsv3418829	copy number variation				No		GRCh38.p12	NC_000017.11	17	60780528	60780537	60790967	60790976	Remapped	1
nstd164	nsv3418830	copy number variation				No		GRCh37 (hg19)	NC_000017.10	17	59272842	59272846	61392993	61392997	Submitted genomic
nstd164	nsv3418830	copy number variation				No		GRCh37 (hg19)	NC_000017.10	17	59272842	59272846	61392993	61392997	Submitted genomic
nstd164	nsv3418830	copy number variation				No		GRCh38.p12	NC_000017.11	17	61195481	61195485	63315632	63315636	Remapped	1

dbVar

Database of genomic structural variation

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