A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610408



Internal ID16397817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12878878..12916449hg38UCSC Ensembl
Innerchr8:12736387..12773958hg19UCSC Ensembl
Innerchr8:12780758..12818329hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3837572
hg1937572
hg1837572
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11988n54
Supporting Variantsnssv1106770
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610408
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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