A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933377



Internal ID22987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49882825..49888424hg38UCSC Ensembl
chr3:49920258..49925857hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5441891
Supporting Variants
Samples
Known GenesMST1R
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933377
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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