A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1125974



Internal ID15979160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:333819..635677hg38UCSC Ensembl
Innerchr9:333819..635677hg19UCSC Ensembl
Innerchr9:323819..625677hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38301859
hg19301859
hg18301859
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613011
Supporting Variants
Samples
Known GenesDOCK8, KANK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1125974
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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