A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526142



Internal ID15453435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:57273804..57700455hg38UCSC Ensembl
Innerchr4:58139970..58566621hg19UCSC Ensembl
Innerchr4:57834727..58261378hg18UCSC Ensembl
Innerchr4:57980898..58407549hg17UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38426652
hg19426652
hg18426652
hg17426652
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv320n21
Supporting Variantsnssv702397
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526142
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer