A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1139758



Internal ID15646258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:97720694..97787971hg38UCSC Ensembl
Innerchr9:100482976..100550253hg19UCSC Ensembl
Innerchr9:99522797..99590074hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3867278
hg1967278
hg1867278
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614934
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)nssv1139758
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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