A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108495



Internal ID22017729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154347246..154396246hg38UCSC Ensembl
chrX:153575614..153624587hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3849001
hg1948974
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642144
Samples
Known GenesEMD, FLNA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108495
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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