A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639590



Internal ID6679681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89624655..89626439hg38UCSC Ensembl
Innerchr16:89624655..89626439hg38UCSC Ensembl
Outerchr16:89624293..89626659hg38UCSC Ensembl
chr16:89691063..89692847hg19UCSC Ensembl
Innerchr16:89691063..89692847hg19UCSC Ensembl
Outerchr16:89690701..89693067hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381785
hg191785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15569842, essv15569843
SamplesNA12718, NA19443
Known GenesDPEP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639590
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer