A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16107446



Internal ID4758606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58077102..58083048hg38UCSC Ensembl
Innerchr19:58077110..58083040hg38UCSC Ensembl
Outerchr19:58077094..58083056hg38UCSC Ensembl
chr19:58588469..58594415hg19UCSC Ensembl
Innerchr19:58588477..58594407hg19UCSC Ensembl
Outerchr19:58588461..58594423hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg385947
hg195947
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644924
Supporting Variants
SamplesNA11829
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16107446
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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