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dbVar

Database of genomic structural variation

nsv4656173

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:162

Description:nsv4520105 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: 104 SVs from 21 studies. See in: genome view

Remapped(Score: Perfect):102,887,964-102,888,125

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4656173	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	102,887,964	102,888,125
nsv4656173	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000002.11	Chr2	103,504,423	103,504,584

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16171120	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16171120	Remapped	Perfect	NC_000002.12:g.102 887964_102888125de l	GRCh38.p12	First Pass	NC_000002.12	Chr2	102,887,964	102,888,125
nssv16171120	Submitted genomic		NC_000002.11:g.103 504423_103504584de l	GRCh37 (hg19)		NC_000002.11	Chr2	103,504,423	103,504,584

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)
nssv16171120	0.012	265	21684

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