A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033142



Internal ID19122364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:42290622..42301188hg38UCSC Ensembl
Innerchr8:42148140..42158706hg19UCSC Ensembl
Innerchr8:42267297..42277863hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3810567
hg1910567
hg1810567
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7185n100
Supporting Variantsnssv3687259, nssv3687261, nssv3687262, nssv3687260
Samples
Known GenesIKBKB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033142
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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