A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16107445



Internal ID5608050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58076104..58079248hg38UCSC Ensembl
Innerchr19:58076105..58079247hg38UCSC Ensembl
Outerchr19:58076103..58079249hg38UCSC Ensembl
chr19:58587472..58590615hg19UCSC Ensembl
Innerchr19:58587473..58590614hg19UCSC Ensembl
Outerchr19:58587471..58590616hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg383145
hg193144
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644923
Supporting Variants
SamplesNA19037
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16107445
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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