A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656341



Internal ID15392993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7177627..7193093hg38UCSC Ensembl
Innerchr5:7177740..7193206hg19UCSC Ensembl
Innerchr5:7230740..7246206hg18UCSC Ensembl
Innerchr5:7230740..7246206hg17UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3815467
hg1915467
hg1815467
hg1715467
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517194
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656341
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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