A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668052



Internal ID15404704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:139606522..139607458hg38UCSC Ensembl
Innerchr4:140527676..140528612hg19UCSC Ensembl
Innerchr4:140747126..140748062hg18UCSC Ensembl
Innerchr4:140885281..140886217hg17UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38937
hg19937
hg18937
hg17937
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515669
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668052
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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