A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15997183



Internal ID5793428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13693616..13695438hg38UCSC Ensembl
Innerchr19:13693626..13695428hg38UCSC Ensembl
Outerchr19:13693606..13695448hg38UCSC Ensembl
chr19:13804430..13806252hg19UCSC Ensembl
Innerchr19:13804440..13806242hg19UCSC Ensembl
Outerchr19:13804420..13806262hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381823
hg191823
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643728
Supporting Variants
SamplesNA19159
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15997183
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