A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16932666



Internal ID22499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48056733..48061905hg38UCSC Ensembl
chr3:48098223..48103395hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg385173
hg195173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5450990
Supporting Variants
Samples
Known GenesMAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16932666
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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