A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016626



Internal ID19105843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139311333..139403743hg38UCSC Ensembl
Innerchr8:140323577..140415986hg19UCSC Ensembl
Innerchr8:140392759..140485168hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3892411
hg1992410
hg1892410
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690066
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016626
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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