A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16967174



Internal ID45429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76191190..76191190hg38UCSC Ensembl
chr5:75487015..75487015hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg382666
hg192666
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5549922
Supporting Variants
Samples
Known GenesSV2C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16967174
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.116562


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