A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16943043



Internal ID29353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184670964..184672029hg38UCSC Ensembl
chr3:184388752..184389817hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg381066
hg191066
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451713
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16943043
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001405


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