A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614972



Internal ID16402381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101843280..101896569hg38UCSC Ensembl
Innerchr9:104605562..104658851hg19UCSC Ensembl
Innerchr9:103645383..103698672hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3853290
hg1953290
hg1853290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12813n54
Supporting Variantsnssv1140278
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614972
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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