A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933892



Internal ID23330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:63816810..63818257hg38UCSC Ensembl
chr3:63802486..63803933hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381448
hg191448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446123
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933892
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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