A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979847



Internal ID22754782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:56473908..56489106hg38UCSC Ensembl
chrX:56500341..56515539hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3815199
hg1915199
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462579
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979847
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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