A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644951



Internal ID7031702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:385214..399104hg38UCSC Ensembl
Innerchr20:385258..399060hg38UCSC Ensembl
Outerchr20:385170..399148hg38UCSC Ensembl
chr20:365858..379748hg19UCSC Ensembl
Innerchr20:365902..379704hg19UCSC Ensembl
Outerchr20:365814..379792hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3813891
hg1913891
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16107594, essv16107595, essv16107596
SamplesNA19725, NA20760, NA20528
Known GenesTRIB3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644951
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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