A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612686



Internal ID16400095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:141850923..141909285hg38UCSC Ensembl
Innerchr8:142932284..142990646hg19UCSC Ensembl
Innerchr8:142930191..142988553hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3858363
hg1958363
hg1858363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12391n54
Supporting Variantsnssv1124907
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612686
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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