A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16932277



Internal ID22241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39956335..39957406hg38UCSC Ensembl
chr3:39997826..39998897hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg381072
hg191072
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5434662
Supporting Variants
Samples
Known GenesMYRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16932277
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.012332


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