A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1140620



Internal ID15993806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103167310..103212472hg38UCSC Ensembl
Innerchr9:105929592..105974754hg19UCSC Ensembl
Innerchr9:104969413..105014575hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3845163
hg1945163
hg1845163
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615042
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)nssv1140620
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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