A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699886



Internal ID15089852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:76870193..76891952hg38UCSC Ensembl
Innerchr5:76166018..76187777hg19UCSC Ensembl
Innerchr5:76201774..76223533hg18UCSC Ensembl
Innerchr5:76201774..76223533hg17UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3821760
hg1921760
hg1821760
hg1721760
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524024
Supporting Variants
Samples
Known GenesS100Z
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699886
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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