A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645042



Internal ID7031793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3496458..3505236hg38UCSC Ensembl
chr20:3477105..3485883hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg388779
hg198779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv772e214
Supporting Variantsessv16121920, essv16121921
SamplesNA19449, HG03084
Known GenesATRN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645042
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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