A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522532



Internal ID15449825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:73160594..73164299hg38UCSC Ensembl
Innerchr5:72456421..72460126hg19UCSC Ensembl
Innerchr5:72492177..72495882hg18UCSC Ensembl
Innerchr5:72492177..72495882hg17UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg383706
hg193706
hg183706
hg173706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705904
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522532
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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