A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5541469



Internal ID316060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34405664..34405664hg38UCSC Ensembl
chr6:34373441..34373441hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982073
Samples
Known GenesRPS10-NUDT3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5541469
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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