A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511202



Internal ID18462797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34933185..35208503hg38UCSC Ensembl
Innerchr10:35222113..35497431hg19UCSC Ensembl
Innerchr10:35262119..35537437hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38275319
hg19275319
hg18275319
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042534
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)nssv3511202
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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