A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17698681



Internal ID122347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96212663..96224157hg38UCSC Ensembl
chr14:96679000..96690494hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3811495
hg1911495
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563175
Supporting Variants
Samples
Known GenesBDKRB2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17698681
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001873


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