A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644160



Internal ID7030916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31986981..31990385hg38UCSC Ensembl
Innerchr19:31986981..31990385hg38UCSC Ensembl
Outerchr19:31986742..31990627hg38UCSC Ensembl
chr19:32477887..32481291hg19UCSC Ensembl
Innerchr19:32477887..32481291hg19UCSC Ensembl
Outerchr19:32477648..32481533hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg383405
hg193405
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16039965
SamplesHG02006
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644160
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer