A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021461



Internal ID19110678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139302765..139447179hg38UCSC Ensembl
Innerchr8:140315009..140459422hg19UCSC Ensembl
Innerchr8:140384191..140528604hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38144415
hg19144414
hg18144414
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7329n100
Supporting Variantsnssv3690064
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)nsv1021461
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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