A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615928



Internal ID16056651
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 StatusM
Merged Variants
Supporting Variantsnssv1148255
Samples
Known GenesCAMSAP1, UBAC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615928
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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