A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16981626



Internal ID55108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42368631..42368654hg38UCSC Ensembl
chr6:42336369..42336392hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5404012
Supporting Variants
Samples
Known GenesTRERF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16981626
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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