A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1134077



Internal ID15640577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39004143..39188240hg38UCSC Ensembl
Innerchr9:39004140..39188237hg19UCSC Ensembl
Innerchr9:38994140..39178237hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38184098
hg19184098
hg18184098
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614282
Supporting Variants
Samples
Known GenesCNTNAP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1134077
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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