A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1128550



Internal ID15981736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11462758..11619839hg38UCSC Ensembl
Innerchr9:11462758..11619839hg19UCSC Ensembl
Innerchr9:11452758..11609839hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38157082
hg19157082
hg18157082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613430
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)nssv1128550
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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