A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611712



Internal ID16399121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:87432473..87472654hg38UCSC Ensembl
Innerchr8:88444701..88484882hg19UCSC Ensembl
Innerchr8:88513817..88553998hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3840182
hg1940182
hg1840182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1117707
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611712
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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