A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15569853



Internal ID2506432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89788160..89810283hg38UCSC Ensembl
Innerchr16:89788660..89809783hg38UCSC Ensembl
Outerchr16:89787160..89811283hg38UCSC Ensembl
chr16:89854568..89876691hg19UCSC Ensembl
Innerchr16:89855068..89876191hg19UCSC Ensembl
Outerchr16:89853568..89877691hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3822124
hg1922124
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639595
Supporting Variants
SamplesHG02224
Known GenesFANCA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15569853
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