A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609990



Internal ID16397399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:6261109..6395711hg38UCSC Ensembl
Innerchr8:6118630..6253232hg19UCSC Ensembl
Innerchr8:6106038..6240640hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38134603
hg19134603
hg18134603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156820
SamplesHGDP01293
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609990
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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