A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16107470



Internal ID6109286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58309412..58314263hg38UCSC Ensembl
Innerchr19:58309427..58314249hg38UCSC Ensembl
Outerchr19:58309398..58314278hg38UCSC Ensembl
chr19:58820778..58825629hg19UCSC Ensembl
Innerchr19:58820793..58825615hg19UCSC Ensembl
Outerchr19:58820764..58825644hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg384852
hg194852
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644933
Supporting Variants
SamplesHG02323
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16107470
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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