A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611882



Internal ID16399291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:110330011..110710240hg38UCSC Ensembl
Innerchr8:111342240..111722469hg19UCSC Ensembl
Innerchr8:111411416..111791645hg18UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg38380230
hg19380230
hg18380230
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1118318
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611882
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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