A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455149



Internal ID233232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34369969..34373323hg38UCSC Ensembl
chr6:34337746..34341100hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg383355
hg193355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982062
Samples
Known GenesNUDT3, RPS10-NUDT3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455149
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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