A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040417



Internal ID18782948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34881487..35027067hg38UCSC Ensembl
Innerchr10:35170415..35315995hg19UCSC Ensembl
Innerchr10:35210421..35356001hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38145581
hg19145581
hg18145581
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv705n100
Supporting Variantsnssv3707752, nssv3513591
Samples
Known GenesCUL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040417
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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