A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7451n54



Internal ID22775346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6045636..6046780hg38UCSC Ensembl
chr20:6026282..6027426hg19UCSC Ensembl
chr20:5974282..5975426hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg381145
hg191145
hg181145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585347, nsv585346, nsv585343, nsv585345, nsv585344
Samples
Known GenesLRRN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7451n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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