A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645764



Internal ID7032512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37641940..37652089hg38UCSC Ensembl
Innerchr20:37641945..37652085hg38UCSC Ensembl
Outerchr20:37641936..37652094hg38UCSC Ensembl
chr20:36270342..36280491hg19UCSC Ensembl
Innerchr20:36270347..36280487hg19UCSC Ensembl
Outerchr20:36270338..36280496hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3810150
hg1910150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16180218
SamplesNA20581
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645764
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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