A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703544



Internal ID15440196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:12261484..12310605hg38UCSC Ensembl
Innerchr5:12261596..12310717hg19UCSC Ensembl
Innerchr5:12314596..12363717hg18UCSC Ensembl
Innerchr5:12314596..12363717hg17UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3849122
hg1949122
hg1849122
hg1749122
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527153
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703544
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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