A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7163n100



Internal ID20158779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38194164..38252697hg38UCSC Ensembl
chr8:38051682..38110215hg19UCSC Ensembl
chr8:38170839..38229372hg18UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3858534
hg1958534
hg1858534
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016845, nsv1022025, nsv1017117, nsv1028308
Samples
Known GenesBAG4, DDHD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7163n100
Frequency
Sample Size29084
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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