A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866290



Internal ID22641225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35690752..35692097hg38UCSC Ensembl
chr14:36159958..36161303hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg381346
hg191346
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455969
Samples
Known GenesRALGAPA1, RALGAPA1P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866290
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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