A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612428



Internal ID16399837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136685592..136835409hg38UCSC Ensembl
Innerchr8:137697835..137847652hg19UCSC Ensembl
Innerchr8:137767017..137916834hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38149818
hg19149818
hg18149818
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12343n54
Supporting Variantsnssv1156195
Samples1782681217_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612428
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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