A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679637



Internal ID15069603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11993121..11993709hg38UCSC Ensembl
Innerchr11:12014668..12015256hg19UCSC Ensembl
Innerchr11:11971244..11971832hg18UCSC Ensembl
Innerchr11:11971244..11971832hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38589
hg19589
hg18589
hg17589
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515847
Supporting Variants
Samples
Known GenesDKK3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679637
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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