A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662039



Internal ID15398691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107785223..107799502hg38UCSC Ensembl
Innerchr11:107655949..107670228hg19UCSC Ensembl
Innerchr11:107161159..107175438hg18UCSC Ensembl
Innerchr11:107161159..107175438hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3814280
hg1914280
hg1814280
hg1714280
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520229
Supporting Variants
Samples
Known GenesSLC35F2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662039
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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