A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16982058



Internal ID55396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34347115..34364638hg38UCSC Ensembl
chr6:34314892..34332415hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3817524
hg1917524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459941
Supporting Variants
Samples
Known GenesNUDT3, RPS10-NUDT3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16982058
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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