A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609494



Internal ID16396903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:1070249..1167739hg38UCSC Ensembl
Innerchr8:1020249..1117739hg19UCSC Ensembl
Innerchr8:1007656..1105146hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3897491
hg1997491
hg1897491
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1103577
Samples
Known GenesERICH1-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609494
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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