A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1139085



Internal ID15992271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:87307957..87317875hg38UCSC Ensembl
Innerchr9:89922872..89932790hg19UCSC Ensembl
Innerchr9:89112692..89122610hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg389919
hg199919
hg189919
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614787
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1139085
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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