A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526873



Internal ID15454166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:14180840..14181580hg38UCSC Ensembl
Innerchr4:14182464..14183204hg19UCSC Ensembl
Innerchr4:13791562..13792302hg18UCSC Ensembl
Innerchr4:13858733..13859473hg17UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38741
hg19741
hg18741
hg17741
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703231
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526873
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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