A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16943598



Internal ID29714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177537445..177537606hg38UCSC Ensembl
chr3:177255233..177255394hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438834
Supporting Variants
Samples
Known GenesLINC00578
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16943598
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003278


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