A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528598



Internal ID15109205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:37803553..37859603hg38UCSC Ensembl
Innerchr8:37661071..37717121hg19UCSC Ensembl
Innerchr8:37780229..37836279hg18UCSC Ensembl
Innerchr8:37780229..37836279hg17UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3856051
hg1956051
hg1856051
hg1756051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705224
Samples
Known GenesBRF2, GPR124, RAB11FIP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528598
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