A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702399



Internal ID15092365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11976348..11977482hg38UCSC Ensembl
Innerchr11:11997895..11999029hg19UCSC Ensembl
Innerchr11:11954471..11955605hg18UCSC Ensembl
Innerchr11:11954471..11955605hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg381135
hg191135
hg181135
hg171135
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526144
Supporting Variants
Samples
Known GenesDKK3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702399
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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