A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593292



Internal ID16034015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1248181..1249785hg38UCSC Ensembl
Innerchr4:1241969..1243573hg19UCSC Ensembl
Innerchr4:1231969..1233573hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381605
hg191605
hg181605
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8893n54
Supporting Variantsnssv987681
Samples
Known GenesCTBP1, CTBP1-AS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593292
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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