A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16938385



Internal ID26320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113491532..113494604hg38UCSC Ensembl
chr3:113210379..113213451hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg383073
hg193073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5445646
Supporting Variants
Samples
Known GenesSPICE1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16938385
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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