A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701613



Internal ID125279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44535143..44535143hg38UCSC Ensembl
chr15:44827341..44827341hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381
hg191
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556361
Supporting Variants
Samples
Known GenesEIF3J-AS1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701613
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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