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dbVar

Database of genomic structural variation

nsv4668748

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:190,567

Description:nsv4602468 from DECIPHER Consensus CNVs. 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: 3175 SVs from 100 studies. See in: genome view

Remapped(Score: Perfect):11,942,480-12,133,046

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4668748	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000009.12	Chr9	11,942,480	12,133,046
nsv4668748	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000009.11	Chr9	11,942,480	12,133,046

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16187644	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv16187644	Remapped	Perfect	NC_000009.12:g.(?_ 11942480)_(1213304 6_?)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,942,480	12,133,046
nssv16187644	Submitted genomic		NC_000009.11:g.(?_ 11942480)_(1213304 6_?)del	GRCh37 (hg19)		NC_000009.11	Chr9	11,942,480	12,133,046

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)
nssv16187644	0.012	10	845

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