A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16002686



Internal ID5189209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15977128..15986116hg38UCSC Ensembl
Innerchr19:15977164..15986081hg38UCSC Ensembl
Outerchr19:15977093..15986152hg38UCSC Ensembl
chr19:16087938..16096926hg19UCSC Ensembl
Innerchr19:16087974..16096891hg19UCSC Ensembl
Outerchr19:16087903..16096962hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg388989
hg198989
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643785
Supporting Variants
SamplesNA18610
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16002686
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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