A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7185n100



Internal ID22793272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42288510..42301240hg38UCSC Ensembl
chr8:42146028..42158758hg19UCSC Ensembl
chr8:42265185..42277915hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3812731
hg1912731
hg1812731
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026040, nsv1015702, nsv1016035, nsv1028114, nsv1020408, nsv1019861, nsv1027854, nsv1033142
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)dgv7185n100
Frequency
Sample Size11257
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


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