A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645450



Internal ID7032200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19092023..19095056hg38UCSC Ensembl
Innerchr20:19092026..19095054hg38UCSC Ensembl
Outerchr20:19092021..19095059hg38UCSC Ensembl
chr20:19072667..19075700hg19UCSC Ensembl
Innerchr20:19072670..19075698hg19UCSC Ensembl
Outerchr20:19072665..19075703hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg383034
hg193034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16154990, essv16154991, essv16154989, essv16154988, essv16154987
SamplesNA18633, HG00610, HG02134, HG02136, HG00463
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645450
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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