A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645449



Internal ID7032199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19076480..19081080hg38UCSC Ensembl
Innerchr20:19076480..19081080hg38UCSC Ensembl
Outerchr20:19075980..19081580hg38UCSC Ensembl
chr20:19057124..19061724hg19UCSC Ensembl
Innerchr20:19057124..19061724hg19UCSC Ensembl
Outerchr20:19056624..19062224hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg384601
hg194601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16154986, essv16154985
SamplesNA21135, NA21109
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645449
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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