A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176142



Internal ID15876123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113612710..113635117hg38UCSC Ensembl
Innerchr9:116374990..116397397hg19UCSC Ensembl
Innerchr9:115414811..115437218hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3822408
hg1922408
hg1822408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615219
Supporting Variants
SamplesHGDP00787
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176142
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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