A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937960



Internal ID26025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:114012178..114012318hg38UCSC Ensembl
chr3:113731025..113731165hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5447612
Supporting Variants
Samples
Known GenesKIAA1407
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937960
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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