A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv927n100



Internal ID19011295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75024700..75329039hg38UCSC Ensembl
chr10:76784458..77088797hg19UCSC Ensembl
chr10:76454464..76758803hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38304340
hg19304340
hg18304340
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051357, nsv1036629
Samples
Known GenesCOMTD1, DUPD1, DUSP13, KAT6B, SAMD8, VDAC2, ZNF503-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv927n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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