A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645460



Internal ID6685522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19760368..19768597hg38UCSC Ensembl
Innerchr20:19760371..19768594hg38UCSC Ensembl
Outerchr20:19760365..19768600hg38UCSC Ensembl
chr20:19741012..19749241hg19UCSC Ensembl
Innerchr20:19741015..19749238hg19UCSC Ensembl
Outerchr20:19741009..19749244hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg388230
hg198230
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16155146
SamplesHG03778
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645460
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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