A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15552494



Internal ID509821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85974881..85980763hg38UCSC Ensembl
Innerchr16:85974881..85980763hg38UCSC Ensembl
Outerchr16:85974582..85980981hg38UCSC Ensembl
chr16:86008487..86014369hg19UCSC Ensembl
Innerchr16:86008487..86014369hg19UCSC Ensembl
Outerchr16:86008188..86014587hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg385883
hg195883
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639472
Supporting Variants
SamplesHG00182
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15552494
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