A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv987673



Internal ID15934943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1247964..1249601hg38UCSC Ensembl
Innerchr4:1241752..1243389hg19UCSC Ensembl
Innerchr4:1231752..1233389hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381638
hg191638
hg181638
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593289
Supporting Variants
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)nssv987673
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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