A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15555140



Internal ID818173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87556986..87565230hg38UCSC Ensembl
Innerchr16:87557017..87565200hg38UCSC Ensembl
Outerchr16:87556956..87565261hg38UCSC Ensembl
chr16:87590592..87598836hg19UCSC Ensembl
Innerchr16:87590623..87598806hg19UCSC Ensembl
Outerchr16:87590562..87598867hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg388245
hg198245
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639518
Supporting Variants
SamplesHG00406
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15555140
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