A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013623



Internal ID18756155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:14334356..14687354hg38UCSC Ensembl
Innerchr4:14335980..14688978hg19UCSC Ensembl
Innerchr4:13945078..14298076hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38352999
hg19352999
hg18352999
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5144n100
Supporting Variantsnssv3619836
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013623
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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