A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17696493



Internal ID120159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35592677..35592701hg38UCSC Ensembl
chr14:36061883..36061907hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3825
hg1925
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559383
Supporting Variants
Samples
Known GenesRALGAPA1, RALGAPA1P
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17696493
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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