A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5675009



Internal ID9741524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62088144..62088523hg38UCSC Ensembl
Outerchr20:62088107..62088573hg38UCSC Ensembl
Innerchr20:60663200..60663579hg19UCSC Ensembl
Outerchr20:60663163..60663629hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2657347
Supporting Variants
SamplesNA19678
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5675009
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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