A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294775



Internal ID20503993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50836513..50836629hg38UCSC Ensembl
chr17:48913874..48913990hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734284
Supporting Variants
Samples
Known GenesWFIKKN2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294775
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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