A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670981



Internal ID15060947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11992070..11995398hg38UCSC Ensembl
Innerchr11:12013617..12016945hg19UCSC Ensembl
Innerchr11:11970193..11973521hg18UCSC Ensembl
Innerchr11:11970193..11973521hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg383329
hg193329
hg183329
hg173329
Variant TypeCNV gain
Copy Number
Allele State
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)nssv670981
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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