A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615029



Internal ID16402438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102315118..102372773hg38UCSC Ensembl
Innerchr9:105077400..105135055hg19UCSC Ensembl
Innerchr9:104117221..104174876hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3857656
hg1957656
hg1857656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176098
SamplesHGDP00003
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615029
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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