A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16971251



Internal ID48179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144018088..144018139hg38UCSC Ensembl
chr6:144339225..144339276hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5401508
Supporting Variants
Samples
Known GenesPLAGL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16971251
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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