A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508083



Internal ID20881381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77990501..78133400hg38UCSC Ensembl
chr16:78024398..78167297hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38142900
hg19142900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032060
Samples
Known GenesCLEC3A, WWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508083
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