A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989006



Internal ID60095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149696782..149696940hg38UCSC Ensembl
chr6:150017918..150018076hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470256
Supporting Variants
Samples
Known GenesLATS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989006
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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