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dbVar

Database of genomic structural variation

nsv6120763

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:374

Description:nsv5504724 from Byrska-Bishop et. al 2021. 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: 111 SVs from 26 studies. See in: genome view

Remapped(Score: Perfect):56,481,579-56,481,952

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6120763	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000012.12	Chr12	56,481,579	56,481,952
nsv6120763	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000012.11	Chr12	56,875,363	56,875,736

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17967128	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17967128	Remapped	Perfect	NC_000012.12:g.564 81579_56481952del	GRCh38.p12	First Pass	NC_000012.12	Chr12	56,481,579	56,481,952
nssv17967128	Submitted genomic		NC_000012.11:g.568 75363_56875736del	GRCh37 (hg19)		NC_000012.11	Chr12	56,875,363	56,875,736

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)
nssv17967128	0.011	67	6322

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