A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528908



Internal ID15456201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:30558467..30563080hg38UCSC Ensembl
Innerchr8:30415984..30420597hg19UCSC Ensembl
Innerchr8:30535526..30540139hg18UCSC Ensembl
Innerchr8:30535526..30540139hg17UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg384614
hg194614
hg184614
hg174614
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705593
Samples
Known GenesRBPMS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528908
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