A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645523



Internal ID7032272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23341978..23347157hg38UCSC Ensembl
Innerchr20:23341978..23347157hg38UCSC Ensembl
Outerchr20:23341859..23347266hg38UCSC Ensembl
chr20:23322615..23327794hg19UCSC Ensembl
Innerchr20:23322615..23327794hg19UCSC Ensembl
Outerchr20:23322496..23327903hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg385180
hg195180
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16163729, essv16163728
SamplesNA19372, HG02580
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645523
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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