A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704614



Internal ID15094580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:87768029..87789546hg38UCSC Ensembl
Innerchr7:87397345..87418861hg19UCSC Ensembl
Innerchr7:87235281..87256797hg18UCSC Ensembl
Innerchr7:87041996..87063512hg17UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3821518
hg1921517
hg1821517
hg1721517
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528078
Supporting Variants
Samples
Known GenesRUNDC3B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704614
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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