A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611531



Internal ID16398940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:72327445..72413168hg38UCSC Ensembl
Innerchr8:73239680..73325403hg19UCSC Ensembl
Innerchr8:73402234..73487957hg18UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3885724
hg1985724
hg1885724
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12198n54
Supporting Variantsnssv1116158
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611531
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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