A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654604



Internal ID15044570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11992266..11994183hg38UCSC Ensembl
Innerchr11:12013813..12015730hg19UCSC Ensembl
Innerchr11:11970389..11972306hg18UCSC Ensembl
Innerchr11:11970389..11972306hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg381918
hg191918
hg181918
hg171918
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)nssv654604
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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