A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526932



Internal ID15454225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:9887140..9887842hg38UCSC Ensembl
Innerchr8:9744650..9745352hg19UCSC Ensembl
Innerchr8:9782060..9782762hg18UCSC Ensembl
Innerchr8:9782060..9782762hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38703
hg19703
hg18703
hg17703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703299
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526932
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