A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17721708



Internal ID145374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14540156..14543600hg38UCSC Ensembl
chr19:14650968..14654412hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg383445
hg193445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5515184
Supporting Variants
Samples
Known GenesTECR
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17721708
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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