A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6341698



Internal ID9584739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:57312838..57317719hg38UCSC Ensembl
Outerchr20:57312801..57317769hg38UCSC Ensembl
Innerchr20:55887894..55892775hg19UCSC Ensembl
Outerchr20:55887857..55892825hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg384969
hg194969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656508
Supporting Variants
SamplesNA19189
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6341698
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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