A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv920n100



Internal ID22787007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68441868..68493125hg38UCSC Ensembl
chr10:70201625..70252882hg19UCSC Ensembl
chr10:69871631..69922888hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3851258
hg1951258
hg1851258
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047078, nsv1043169
Samples
Known GenesDNA2, SLC25A16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv920n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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