A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv245n21



Internal ID22766437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:41335690..41359612hg38UCSC Ensembl
chr20:39964330..39988252hg19UCSC Ensembl
chr20:39397744..39421666hg18UCSC Ensembl
chr20:39397744..39421666hg17UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3823923
hg1923923
hg1823923
hg1723923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv516924, nsv527136
Samples
Known GenesLPIN3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv245n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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