A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16939543



Internal ID27080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127288148..127288204hg38UCSC Ensembl
chr3:127006991..127007047hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449831
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16939543
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.007805


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