A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662617



Internal ID15399269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107785223..107793943hg38UCSC Ensembl
Innerchr11:107655949..107664669hg19UCSC Ensembl
Innerchr11:107161159..107169879hg18UCSC Ensembl
Innerchr11:107161159..107169879hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg388721
hg198721
hg188721
hg178721
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)nssv662617
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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