A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021643



Internal ID19110861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:43529945..43968893hg38UCSC Ensembl
Innerchr8:43385088..43824036hg19UCSC Ensembl
Innerchr8:43504245..43943193hg18UCSC Ensembl
Cytoband8p11.1
Allele length
AssemblyAllele length
hg38438949
hg19438949
hg18438949
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7189n100
Supporting Variantsnssv3687282, nssv3687283, nssv3687281, nssv3687284, nssv3687280
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)nsv1021643
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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