A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977776



Internal ID52575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180410459..180410501hg38UCSC Ensembl
chr5:179837459..179837501hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534857
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977776
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.035714


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