A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645738



Internal ID6685799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36548670..36555667hg38UCSC Ensembl
Innerchr20:36548687..36555650hg38UCSC Ensembl
Outerchr20:36548653..36555684hg38UCSC Ensembl
chr20:35177073..35184070hg19UCSC Ensembl
Innerchr20:35177090..35184053hg19UCSC Ensembl
Outerchr20:35177056..35184087hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg386998
hg196998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16179811, essv16179812
SamplesNA19917, HG00105
Known GenesMYL9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645738
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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