A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688371



Internal ID15425023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:112732761..112742949hg38UCSC Ensembl
Innerchr4:113653917..113664105hg19UCSC Ensembl
Innerchr4:113873366..113883554hg18UCSC Ensembl
Innerchr4:114011521..114021709hg17UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3810189
hg1910189
hg1810189
hg1710189
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520766
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688371
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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