A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526211



Internal ID15106818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:85745740..85755954hg38UCSC Ensembl
Innerchr4:86666893..86677107hg19UCSC Ensembl
Innerchr4:86885917..86896131hg18UCSC Ensembl
Innerchr4:87024072..87034286hg17UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg3810215
hg1910215
hg1810215
hg1710215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702475
Samples
Known GenesARHGAP24
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526211
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