A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3508629



Internal ID18806910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:122712293..122818935hg38UCSC Ensembl
Innerchr11:122583001..122689643hg19UCSC Ensembl
Innerchr11:122088211..122194853hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38106643
hg19106643
hg18106643
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039632
Supporting Variants
Samples
Known GenesUBASH3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3508629
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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