A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17694791



Internal ID118457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:47994837..48039650hg38UCSC Ensembl
chr14:48464040..48508853hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3844814
hg1944814
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558905
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17694791
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000624


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