A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611982



Internal ID16399391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:114455006..114493941hg38UCSC Ensembl
Innerchr8:115467235..115506170hg19UCSC Ensembl
Innerchr8:115536411..115575346hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3838936
hg1938936
hg1838936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156382
SamplesHGDP00647
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611982
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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