A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646074



Internal ID7032819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51918356..51921618hg38UCSC Ensembl
Innerchr20:51918356..51921618hg38UCSC Ensembl
Outerchr20:51917856..51922118hg38UCSC Ensembl
chr20:50534895..50538157hg19UCSC Ensembl
Innerchr20:50534895..50538157hg19UCSC Ensembl
Outerchr20:50534395..50538657hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg383263
hg193263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16199723
SamplesHG01777
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646074
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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