A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522868



Internal ID15450161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25688240..25794084hg38UCSC Ensembl
Innerchr8:25545756..25651600hg19UCSC Ensembl
Innerchr8:25601673..25707517hg18UCSC Ensembl
Innerchr8:25601673..25707517hg17UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38105845
hg19105845
hg18105845
hg17105845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv455n21
Supporting Variantsnssv698523
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522868
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