A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15373008



Internal ID5374824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10279657..10355874hg38UCSC Ensembl
chr16:10373514..10449731hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3876218
hg1976218
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637893
Supporting Variants
SamplesHG01974
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15373008
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