A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16013660



Internal ID6015476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:22596307..22597674hg38UCSC Ensembl
Innerchr19:22596307..22597674hg38UCSC Ensembl
Outerchr19:22595946..22597945hg38UCSC Ensembl
chr19:22779109..22780476hg19UCSC Ensembl
Innerchr19:22779109..22780476hg19UCSC Ensembl
Outerchr19:22778748..22780747hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381368
hg191368
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643958
Supporting Variants
SamplesHG02107
Known GenesLOC440518
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16013660
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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