A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703962



Internal ID15440614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:120362021..120388374hg38UCSC Ensembl
Innerchr5:119697716..119724069hg19UCSC Ensembl
Innerchr5:119725615..119751968hg18UCSC Ensembl
Innerchr5:119725615..119751968hg17UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3826354
hg1926354
hg1826354
hg1726354
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527509
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703962
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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