A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7162n100



Internal ID20158778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38159377..38249049hg38UCSC Ensembl
chr8:38016895..38106567hg19UCSC Ensembl
chr8:38136052..38225724hg18UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3889673
hg1989673
hg1889673
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022629, nsv1018802
Samples
Known GenesBAG4, DDHD2, LSM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7162n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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