A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611370



Internal ID16398779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:53208794..53210701hg38UCSC Ensembl
Innerchr8:54121354..54123261hg19UCSC Ensembl
Innerchr8:54283907..54285814hg18UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg381908
hg191908
hg181908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12170n54
Supporting Variantsnssv1115460, nssv1115461
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611370
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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