A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16982072



Internal ID55405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34403961..34404493hg38UCSC Ensembl
chr6:34371738..34372270hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473408
Supporting Variants
Samples
Known GenesRPS10-NUDT3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16982072
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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