A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1134719



Internal ID15987905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63070849..63096908hg38UCSC Ensembl
Innerchr9:66975821..67001880hg19UCSC Ensembl
Innerchr9:66715641..66741700hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3826060
hg1926060
hg1826060
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614519
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)nssv1134719
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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