A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16039966



Internal ID3096823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32065127..32066373hg38UCSC Ensembl
Innerchr19:32065135..32066366hg38UCSC Ensembl
Outerchr19:32065120..32066381hg38UCSC Ensembl
chr19:32556033..32557279hg19UCSC Ensembl
Innerchr19:32556041..32557272hg19UCSC Ensembl
Outerchr19:32556026..32557287hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381247
hg191247
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644161
Supporting Variants
SamplesHG02722
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16039966
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