A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1128563



Internal ID15981749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11651144..11835471hg38UCSC Ensembl
Innerchr9:11651144..11835471hg19UCSC Ensembl
Innerchr9:11641144..11825471hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38184328
hg19184328
hg18184328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613440
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)nssv1128563
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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