A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611371



Internal ID16398780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:53208794..53211002hg38UCSC Ensembl
Innerchr8:54121354..54123562hg19UCSC Ensembl
Innerchr8:54283907..54286115hg18UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg382209
hg192209
hg182209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12170n54
Supporting Variantsnssv1115462, nssv1115465, nssv1115466, nssv1115464, nssv1115463
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611371
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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