A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17696188



Internal ID119854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51758124..51771714hg38UCSC Ensembl
chr14:52224842..52238432hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3813591
hg1913591
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555055
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17696188
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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