A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929005



Internal ID20047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3370319..3376964hg38UCSC Ensembl
chr3:3412003..3418648hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg386646
hg196646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451656
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929005
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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