A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977198



Internal ID52193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:174114343..174114343hg38UCSC Ensembl
chr5:173541346..173541346hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38768
hg19768
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547544
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977198
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.42942


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