A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985962



Internal ID58055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55143121..55143121hg38UCSC Ensembl
chr6:55007919..55007919hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5549832
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985962
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.202965


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