A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700622



Internal ID15437274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:57215424..57837344hg38UCSC Ensembl
Innerchr4:58081590..58703510hg19UCSC Ensembl
Innerchr4:57776347..58398267hg18UCSC Ensembl
Innerchr4:57922518..58544438hg17UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38621921
hg19621921
hg18621921
hg17621921
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524655
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700622
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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