A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527184



Internal ID15454477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10672527..10732403hg38UCSC Ensembl
Innerchr8:10530037..10589913hg19UCSC Ensembl
Innerchr8:10567447..10627323hg18UCSC Ensembl
Innerchr8:10567447..10627323hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3859877
hg1959877
hg1859877
hg1759877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703580
Samples
Known GenesC8orf74, SOX7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527184
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