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dbVar

Database of genomic structural variation

nsv4658926

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:7,550

Description:nsv4588270 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: 118 SVs from 33 studies. See in: genome view

Remapped(Score: Perfect):190,066,540-190,074,089

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4658926	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	190,066,540	190,074,089
nsv4658926	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	190,987,695	190,995,244

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16182984	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv16182984	Remapped	Perfect	NC_000004.12:g.(?_ 190066540)_(190074 089_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	190,066,540	190,074,089
nssv16182984	Submitted genomic		NC_000004.11:g.(?_ 190987695)_(190995 244_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	190,987,695	190,995,244

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)
nssv16182984	0.013	11	845

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