A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645155



Internal ID7031906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:7971350..7974849hg38UCSC Ensembl
Innerchr20:7971350..7974849hg38UCSC Ensembl
Outerchr20:7970850..7975349hg38UCSC Ensembl
chr20:7951997..7955496hg19UCSC Ensembl
Innerchr20:7951997..7955496hg19UCSC Ensembl
Outerchr20:7951497..7955996hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16134019, essv16134020
SamplesHG01344, NA19083
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645155
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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