A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16007576



Internal ID3574954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20413029..20535144hg38UCSC Ensembl
Innerchr19:20413029..20535144hg38UCSC Ensembl
Outerchr19:20413029..20535144hg38UCSC Ensembl
chr19:20595835..20717950hg19UCSC Ensembl
Innerchr19:20595835..20717950hg19UCSC Ensembl
Outerchr19:20595835..20717950hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38122116
hg19122116
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643884
Supporting Variants
SamplesHG03163
Known GenesZNF826P
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16007576
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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