A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv20n21



Internal ID20131741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:184614160..184627450hg38UCSC Ensembl
chr1:184583294..184596584hg19UCSC Ensembl
chr1:182849917..182863207hg18UCSC Ensembl
chr1:181314951..181328241hg17UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3813291
hg1913291
hg1813291
hg1713291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv525959, nsv528925
Samples
Known GenesC1orf21
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv20n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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