A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17696468



Internal ID120134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71236114..71236116hg38UCSC Ensembl
chr14:71702831..71702833hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg383
hg193
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556716
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17696468
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000937


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