A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690012



Internal ID15079978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11993121..11995398hg38UCSC Ensembl
Innerchr11:12014668..12016945hg19UCSC Ensembl
Innerchr11:11971244..11973521hg18UCSC Ensembl
Innerchr11:11971244..11973521hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg382278
hg192278
hg182278
hg172278
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)nssv690012
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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