A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624423



Internal ID21816470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74372145..74443308hg38UCSC Ensembl
chr16:74406043..74477206hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3871164
hg1971164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6030267
Supporting Variants
Samples
Known GenesCLEC18B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624423
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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