A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv926n100



Internal ID20152542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74994872..75081593hg38UCSC Ensembl
chr10:76754630..76841351hg19UCSC Ensembl
chr10:76424636..76511357hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3886722
hg1986722
hg1886722
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047034, nsv1049149, nsv1038957
Samples
Known GenesDUPD1, KAT6B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv926n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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