A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3514760



Internal ID18466355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34777173..35027067hg38UCSC Ensembl
Innerchr10:35066101..35315995hg19UCSC Ensembl
Innerchr10:35106107..35356001hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38249895
hg19249895
hg18249895
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043070
Supporting Variants
Samples
Known GenesCUL2, PARD3, PARD3-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3514760
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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