A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508216



Internal ID20881515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87674225..87676982hg38UCSC Ensembl
chr16:87707831..87710588hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg382758
hg192758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033651
Samples
Known GenesJPH3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508216
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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