A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv37n21



Internal ID22766229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12024028..12123248hg38UCSC Ensembl
chr10:12066027..12165247hg19UCSC Ensembl
chr10:12106033..12205253hg18UCSC Ensembl
chr10:12106033..12205253hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3899221
hg1999221
hg1899221
hg1799221
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv519115, nsv515591
Samples
Known GenesDHTKD1, UPF2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv37n21
Frequency
Sample Size2026
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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