A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1140595



Internal ID15993781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101998200..102117417hg38UCSC Ensembl
Innerchr9:104760482..104879699hg19UCSC Ensembl
Innerchr9:103800303..103919520hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38119218
hg19119218
hg18119218
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615012
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)nssv1140595
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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