A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526818



Internal ID15454111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:28911730..28914626hg38UCSC Ensembl
Innerchr8:28769247..28772143hg19UCSC Ensembl
Innerchr8:28825166..28828062hg18UCSC Ensembl
Innerchr8:28825166..28828062hg17UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg382897
hg192897
hg182897
hg172897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703172
Samples
Known GenesHMBOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526818
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