A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3520117



Internal ID18471712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34893474..35230186hg38UCSC Ensembl
Innerchr10:35182402..35519114hg19UCSC Ensembl
Innerchr10:35222408..35559120hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38336713
hg19336713
hg18336713
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053665
Supporting Variants
Samples
Known GenesCREM, CUL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3520117
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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