A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610177



Internal ID16397586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8461340..8597021hg38UCSC Ensembl
Innerchr8:8318850..8454531hg19UCSC Ensembl
Innerchr8:8356260..8491941hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38135682
hg19135682
hg18135682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11939n54
Supporting Variantsnssv1105935
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610177
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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