A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594121



Internal ID20967192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35757197..35758052hg38UCSC Ensembl
chr14:36226403..36227258hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38856
hg19856
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223171
Samples
Known GenesRALGAPA1, RALGAPA1P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594121
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer