A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126224



Internal ID15979410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:3061261..3120123hg38UCSC Ensembl
Innerchr9:3061261..3120123hg19UCSC Ensembl
Innerchr9:3051261..3110123hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3858863
hg1958863
hg1858863
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613144
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)nssv1126224
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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