A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610598



Internal ID16051321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16129350..16171585hg38UCSC Ensembl
Innerchr8:15986859..16029094hg19UCSC Ensembl
Innerchr8:16031230..16073465hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3842236
hg1942236
hg1842236
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12025n54
Supporting Variantsnssv1156341
SamplesHGDP01172
Known GenesMSR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610598
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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