A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7677n54



Internal ID18999853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63736025..63738644hg38UCSC Ensembl
chr20:62367377..62369997hg19UCSC Ensembl
chr20:61837821..61840441hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382620
hg192621
hg182621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586616, nsv586617
Samples
Known GenesLIME1, ZGPAT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7677n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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