A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5873161



Internal ID9007564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:50986045..50990566hg38UCSC Ensembl
Outerchr20:50986008..50990616hg38UCSC Ensembl
Innerchr20:49602582..49607103hg19UCSC Ensembl
Outerchr20:49602545..49607153hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg384609
hg194609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659875
Supporting Variants
SamplesHG00614
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5873161
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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