A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940117



Internal ID27456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158586168..158586285hg38UCSC Ensembl
chr3:158303957..158304074hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5448433
Supporting Variants
Samples
Known GenesMLF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940117
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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