A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588899



Internal ID20961970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35718761..35719980hg38UCSC Ensembl
chr14:36187967..36189186hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg381220
hg191220
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228150
Samples
Known GenesRALGAPA1, RALGAPA1P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588899
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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