A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665282



Internal ID9931387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36415226..36427439hg38UCSC Ensembl
chr20:35043629..35055842hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3812214
hg1912214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6360840, essv6321706
SamplesHG00607, HG00421
Known GenesDLGAP4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665282
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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