A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16006932



Internal ID4520400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19824168..19828006hg38UCSC Ensembl
Innerchr19:19824169..19828005hg38UCSC Ensembl
Outerchr19:19824167..19828007hg38UCSC Ensembl
chr19:19934977..19938815hg19UCSC Ensembl
Innerchr19:19934978..19938814hg19UCSC Ensembl
Outerchr19:19934976..19938816hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg383839
hg193839
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643859
Supporting Variants
SamplesHG04019
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16006932
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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