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dbVar

Database of genomic structural variation

nsv4646830

Organism: Homo sapiens

Study:nstd186 (NCBI Curated Common Structural Variants)
Variant Type:copy number variation
Method Type:Curated
Submitted on:GRCh37

Variant Calls:4
Validation:Not tested
Clinical Assertions: No
Region Size:21,001

Description:nsv4051924 from gnomAD Structural Variants. For a full list of variants now included in nstd186, refer to the mapping file provided here.

Links to Other Resources

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 293 SVs from 64 studies. See in: genome view

Remapped(Score: Perfect):155,213,709-155,234,709

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4646830	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	155,213,709	155,234,709
nsv4646830	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	155,183,500	155,204,500

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16163213	copy number variation	Curated	Curated
nssv16163824	copy number variation	Curated	Curated
nssv16169051	copy number variation	Curated	Curated
nssv16181343	copy number variation	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16163213	Remapped	Perfect	GRCh38.p12	First Pass	NC_000001.11	Chr1	155,213,709	155,234,709
nssv16163824	Remapped	Perfect	GRCh38.p12	First Pass	NC_000001.11	Chr1	155,213,709	155,234,709
nssv16169051	Remapped	Perfect	GRCh38.p12	First Pass	NC_000001.11	Chr1	155,213,709	155,234,709
nssv16181343	Remapped	Perfect	GRCh38.p12	First Pass	NC_000001.11	Chr1	155,213,709	155,234,709
nssv16163213	Submitted genomic		GRCh37 (hg19)		NC_000001.10	Chr1	155,183,500	155,204,500
nssv16163824	Submitted genomic		GRCh37 (hg19)		NC_000001.10	Chr1	155,183,500	155,204,500
nssv16169051	Submitted genomic		GRCh37 (hg19)		NC_000001.10	Chr1	155,183,500	155,204,500
nssv16181343	Submitted genomic		GRCh37 (hg19)		NC_000001.10	Chr1	155,183,500	155,204,500

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv16163213	0.015	161	10847
nssv16163824	0.018	200	10847
nssv16169051	0.024	263	10847
nssv16181343	0.929	10076	10847

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