A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046128



Internal ID18788659
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 StatusM
Merged Variantsdgv706n100
Supporting Variantsnssv3517791
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)nsv1046128
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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