A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646297



Internal ID7033042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62847710..62848185hg38UCSC Ensembl
Innerchr20:62847763..62848132hg38UCSC Ensembl
Outerchr20:62847657..62848238hg38UCSC Ensembl
chr20:61479062..61479537hg19UCSC Ensembl
Innerchr20:61479115..61479484hg19UCSC Ensembl
Outerchr20:61479009..61479590hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16222269
SamplesHG02679
Known GenesTCFL5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646297
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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