A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644995



Internal ID7031746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2073089..2077567hg38UCSC Ensembl
Innerchr20:2073169..2077487hg38UCSC Ensembl
Outerchr20:2073009..2077647hg38UCSC Ensembl
chr20:2053735..2058213hg19UCSC Ensembl
Innerchr20:2053815..2058133hg19UCSC Ensembl
Outerchr20:2053655..2058293hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg384479
hg194479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16119023
SamplesNA18602
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644995
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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