A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663137



Internal ID15399789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:124738263..124754029hg38UCSC Ensembl
Innerchr8:125750505..125766271hg19UCSC Ensembl
Innerchr8:125819686..125835452hg18UCSC Ensembl
Innerchr8:125819686..125835452hg17UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3815767
hg1915767
hg1815767
hg1715767
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517427
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663137
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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