A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615052



Internal ID16402461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103715214..103796936hg38UCSC Ensembl
Innerchr9:106477496..106559217hg19UCSC Ensembl
Innerchr9:105517317..105599038hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3881723
hg1981722
hg1881722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176105
Samples1782681096_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615052
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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