A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv962426



Internal ID15909696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41843258..42115297hg38UCSC Ensembl
Innerchr3:41884750..42156789hg19UCSC Ensembl
Innerchr3:41859754..42131793hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38272040
hg19272040
hg18272040
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590139
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)nssv962426
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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