A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16938387



Internal ID26322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113508191..113515053hg38UCSC Ensembl
chr3:113227038..113233900hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg386863
hg196863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446669
Supporting Variants
Samples
Known GenesSPICE1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16938387
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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