A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7683n54



Internal ID20141107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63737667..63741603hg38UCSC Ensembl
chr20:62369020..62372956hg19UCSC Ensembl
chr20:61839464..61843400hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg383937
hg193937
hg183937
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586632, nsv586634
Samples
Known GenesLIME1, SLC2A4RG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7683n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss2
Observed Complex0
Frequencyn/a


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