A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524655



Internal ID15451948
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700622
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524655
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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