A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv34n21



Internal ID22766226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:741956..756332hg38UCSC Ensembl
chr10:787896..802272hg19UCSC Ensembl
chr10:777896..792272hg18UCSC Ensembl
chr10:777896..792272hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3814377
hg1914377
hg1814377
hg1714377
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv521935, nsv525722
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv34n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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