A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001981



Internal ID21911324
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 StatusM
Merged Variants
Supporting Variantsnssv17558941
Samples
Known GenesSLC35B3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001981
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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