A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689749



Internal ID18988030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:101371556..101390702hg38UCSC Ensembl
Innerchr8:102383784..102402930hg19UCSC Ensembl
Innerchr8:102452960..102472106hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3819147
hg1919147
hg1819147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025254
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3689749
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer