A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17698654



Internal ID122320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95687827..95689163hg38UCSC Ensembl
chr14:96154164..96155500hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg381337
hg191337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513287
Supporting Variants
Samples
Known GenesTCL1B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17698654
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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