A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148255



Internal ID15654755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135885466..136002028hg38UCSC Ensembl
Innerchr9:138777312..138893874hg19UCSC Ensembl
Innerchr9:137917133..138033695hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38116563
hg19116563
hg18116563
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615928
Supporting Variants
Samples
Known GenesCAMSAP1, UBAC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148255
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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