A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850026



Internal ID22624961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35719146..35720745hg38UCSC Ensembl
chr14:36188352..36189951hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452167
Samples
Known GenesRALGAPA1, RALGAPA1P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850026
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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