A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6466892



Internal ID9699182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:3495472..3505340hg38UCSC Ensembl
Outerchr20:3495435..3505390hg38UCSC Ensembl
Innerchr20:3476119..3485987hg19UCSC Ensembl
Outerchr20:3476082..3486037hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg389956
hg199956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664121
Supporting Variants
SamplesNA19449
Known GenesATRN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6466892
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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