A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7140n100



Internal ID19017508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23381854..23440564hg38UCSC Ensembl
chr8:23239367..23298077hg19UCSC Ensembl
chr8:23295312..23354022hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3858711
hg1958711
hg1858711
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034639, nsv1023053
Samples
Known GenesENTPD4, LOXL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7140n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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