A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3517791



Internal ID18469386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34881487..35204961hg38UCSC Ensembl
Innerchr10:35170415..35493889hg19UCSC Ensembl
Innerchr10:35210421..35533895hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38323475
hg19323475
hg18323475
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046128
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)nssv3517791
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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