A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126871



Internal ID15980057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:8009428..8097977hg38UCSC Ensembl
Innerchr9:8009428..8097977hg19UCSC Ensembl
Innerchr9:7999428..8087977hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3888550
hg1988550
hg1888550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613279
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)nssv1126871
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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