A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16179811



Internal ID6181627
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645738
Supporting Variants
SamplesHG00105
Known GenesMYL9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16179811
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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