A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7591n54



Internal ID20141015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45722456..45734110hg38UCSC Ensembl
chr20:44351095..44362749hg19UCSC Ensembl
chr20:43784509..43796156hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3811655
hg1911655
hg1811648
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586122, nsv586126, nsv586127
Samples
Known GenesSPINT4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7591n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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