A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705675



Internal ID15095641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67457517..67459535hg38UCSC Ensembl
Innerchr11:67224988..67227006hg19UCSC Ensembl
Innerchr11:66981564..66983582hg18UCSC Ensembl
Innerchr11:66981564..66983582hg17UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382019
hg192019
hg182019
hg172019
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528976
Supporting Variants
Samples
Known GenesCABP4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705675
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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