A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17686434



Internal ID110100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27583224..27583228hg38UCSC Ensembl
chr13:28157361..28157365hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5539197
Supporting Variants
Samples
Known GenesLNX2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17686434
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.047612


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