A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv374n21



Internal ID22766566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22036638..22044787hg38UCSC Ensembl
chr6:22036867..22045016hg19UCSC Ensembl
chr6:22144846..22152995hg18UCSC Ensembl
chr6:22144846..22152995hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg388150
hg198150
hg188150
hg178150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523982, nsv520732
Samples
Known GenesCASC15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv374n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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