A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611907



Internal ID16399316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:111965150..112048403hg38UCSC Ensembl
Innerchr8:112977379..113060632hg19UCSC Ensembl
Innerchr8:113046555..113129808hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3883254
hg1983254
hg1883254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156374
SamplesHGDP01347
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611907
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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