A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7684n54



Internal ID22775579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63738644..63789659hg38UCSC Ensembl
chr20:62369997..62421012hg19UCSC Ensembl
chr20:61840441..61891456hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3851016
hg1951016
hg1851016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586645, nsv586642
SamplesNINDS_119, HGDP00655
Known GenesLIME1, SLC2A4RG, ZBTB46
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7684n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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