A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7082n100



Internal ID22793169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:12616022..12720569hg38UCSC Ensembl
chr8:12473531..12578078hg19UCSC Ensembl
chr8:12517902..12622449hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38104548
hg19104548
hg18104548
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022410, nsv1033682, nsv1019027
Samples
Known GenesLOC729732
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7082n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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