A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7682n54



Internal ID22775577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63737667..63740090hg38UCSC Ensembl
chr20:62369020..62371443hg19UCSC Ensembl
chr20:61839464..61841887hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382424
hg192424
hg182424
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586629, nsv586641, nsv586630, nsv586636
Samples
Known GenesLIME1, SLC2A4RG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7682n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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