A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558941



Internal ID21883296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8432262..8434992hg38UCSC Ensembl
chr6:8432495..8435225hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg382731
hg192731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6001981
Supporting Variants
Samples
Known GenesSLC35B3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558941
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