A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1128564



Internal ID15981750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11651144..11934943hg38UCSC Ensembl
Innerchr9:11651144..11934943hg19UCSC Ensembl
Innerchr9:11641144..11924943hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38283800
hg19283800
hg18283800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613441
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)nssv1128564
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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