A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019861



Internal ID19109079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:42288510..42300658hg38UCSC Ensembl
Innerchr8:42146028..42158176hg19UCSC Ensembl
Innerchr8:42265185..42277333hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3812149
hg1912149
hg1812149
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7185n100
Supporting Variantsnssv3687248
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)nsv1019861
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