A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517921



Internal ID15445214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:81394316..81425681hg38UCSC Ensembl
Innerchr4:82315470..82346835hg19UCSC Ensembl
Innerchr4:82534494..82565859hg18UCSC Ensembl
Innerchr4:82672649..82704014hg17UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3831366
hg1931366
hg1831366
hg1731366
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695332
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517921
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