A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710756



Internal ID18662351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119424353..119535659hg38UCSC Ensembl
Innerchr11:119295063..119406369hg19UCSC Ensembl
Innerchr11:118800273..118911579hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38111307
hg19111307
hg18111307
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054222
Supporting Variants
Samples
Known GenesUSP2-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3710756
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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