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dbVar

Database of genomic structural variation

nsv4636261

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:98

Description:nsv4037751 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: 152 SVs from 40 studies. See in: genome view

Remapped(Score: Perfect):45,517,814-45,517,911

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4636261	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	45,517,814	45,517,911
nsv4636261	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	45,983,486	45,983,583

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16161020	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16161020	Remapped	Perfect	NC_000001.11:g.455 17814_45517911del	GRCh38.p12	First Pass	NC_000001.11	Chr1	45,517,814	45,517,911
nssv16161020	Submitted genomic		NC_000001.10:g.459 83486_45983583del	GRCh37 (hg19)		NC_000001.10	Chr1	45,983,486	45,983,583

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)
nssv16161020	0.367	7928	21594

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