A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705007



Internal ID15094973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:558884..620599hg38UCSC Ensembl
Innerchr11:558884..620599hg19UCSC Ensembl
Innerchr11:548884..610599hg18UCSC Ensembl
Innerchr11:548884..610599hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3861716
hg1961716
hg1861716
hg1761716
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528415
Supporting Variants
Samples
Known GenesC11orf35, CDHR5, IRF7, LOC143666, MIR210, MIR210HG, PHRF1, RASSF7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705007
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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