A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16982341



Internal ID55575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25921803..25921842hg38UCSC Ensembl
chr6:25922031..25922070hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5537934
Supporting Variants
Samples
Known GenesSLC17A2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16982341
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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