A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644295



Internal ID7031051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37798850..37803408hg38UCSC Ensembl
Innerchr19:37798900..37803358hg38UCSC Ensembl
Outerchr19:37798800..37803458hg38UCSC Ensembl
chr19:38289490..38294048hg19UCSC Ensembl
Innerchr19:38289540..38293998hg19UCSC Ensembl
Outerchr19:38289440..38294098hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg384559
hg194559
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16051976, essv16051977
SamplesHG00101, NA20785
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644295
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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