A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16978018



Internal ID52750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3355949..3355980hg38UCSC Ensembl
chr6:3356183..3356214hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5412967
Supporting Variants
Samples
Known GenesSLC22A23
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16978018
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003287


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