A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1128572



Internal ID15981758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11745912..12220126hg38UCSC Ensembl
Innerchr9:11745912..12220126hg19UCSC Ensembl
Innerchr9:11735912..12210126hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38474215
hg19474215
hg18474215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613449
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)nssv1128572
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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