A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16178065



Internal ID6179881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34653922..34656669hg38UCSC Ensembl
Innerchr20:34654422..34656169hg38UCSC Ensembl
Outerchr20:34652922..34657669hg38UCSC Ensembl
chr20:33241726..33244473hg19UCSC Ensembl
Innerchr20:33242226..33243973hg19UCSC Ensembl
Outerchr20:33240726..33245473hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg382748
hg192748
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645704
Supporting Variants
SamplesNA19397
Known GenesPIGU
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16178065
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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