A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17734917



Internal ID158583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101822315..101824257hg38UCSC Ensembl
chr3:101541159..101543101hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg381943
hg191943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5450154
Supporting Variants
Samples
Known GenesNXPE3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17734917
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001561


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