A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526815



Internal ID15454108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:132426605..132436049hg38UCSC Ensembl
Innerchr4:133347760..133357204hg19UCSC Ensembl
Innerchr4:133567210..133576654hg18UCSC Ensembl
Innerchr4:133705365..133714809hg17UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg389445
hg199445
hg189445
hg179445
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703169
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526815
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