A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697910



Internal ID15434562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:10710604..10727527hg38UCSC Ensembl
Innerchr5:10710716..10727639hg19UCSC Ensembl
Innerchr5:10763716..10780639hg18UCSC Ensembl
Innerchr5:10763716..10780639hg17UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3816924
hg1916924
hg1816924
hg1716924
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521304
Supporting Variants
Samples
Known GenesDAP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697910
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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