A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610406



Internal ID16051129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12840048..12975127hg38UCSC Ensembl
Innerchr8:12697557..12832636hg19UCSC Ensembl
Innerchr8:12741928..12877007hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38135080
hg19135080
hg18135080
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1106768
Samples
Known GenesKIAA1456
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610406
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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