A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696719



Internal ID15433371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:94356160..94371551hg38UCSC Ensembl
Innerchr4:95277311..95292702hg19UCSC Ensembl
Innerchr4:95496334..95511725hg18UCSC Ensembl
Innerchr4:95634489..95649880hg17UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3815392
hg1915392
hg1815392
hg1715392
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519228
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696719
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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