A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1140597



Internal ID15647097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102112702..102232627hg38UCSC Ensembl
Innerchr9:104874984..104994909hg19UCSC Ensembl
Innerchr9:103914805..104034730hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38119926
hg19119926
hg18119926
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615017
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)nssv1140597
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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