A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645762



Internal ID7032510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37571596..37575468hg38UCSC Ensembl
Innerchr20:37571611..37575453hg38UCSC Ensembl
Outerchr20:37571581..37575483hg38UCSC Ensembl
chr20:36199998..36203870hg19UCSC Ensembl
Innerchr20:36200013..36203855hg19UCSC Ensembl
Outerchr20:36199983..36203885hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg383873
hg193873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16180216
SamplesNA19430
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645762
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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