A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610271



Internal ID16397680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10581286..10601693hg38UCSC Ensembl
Innerchr8:10438796..10459203hg19UCSC Ensembl
Innerchr8:10476206..10496613hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3820408
hg1920408
hg1820408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1106255
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610271
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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