A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv962431



Internal ID15909701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41918514..42142869hg38UCSC Ensembl
Innerchr3:41960006..42184361hg19UCSC Ensembl
Innerchr3:41935010..42159365hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38224356
hg19224356
hg18224356
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590146
Supporting Variants
Samples
Known GenesTRAK1, ULK4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv962431
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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