A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931689



Internal ID21863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44340603..44345351hg38UCSC Ensembl
chr3:44382095..44386843hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg384749
hg194749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451848
Supporting Variants
Samples
Known GenesTCAIM
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931689
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003903


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