A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16109563



Internal ID5994098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1092622..1096681hg38UCSC Ensembl
Innerchr20:1092622..1096681hg38UCSC Ensembl
Outerchr20:1092497..1096783hg38UCSC Ensembl
chr20:1073265..1077324hg19UCSC Ensembl
Innerchr20:1073265..1077324hg19UCSC Ensembl
Outerchr20:1073140..1077426hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg384060
hg194060
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644972
Supporting Variants
SamplesNA19395
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16109563
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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