A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463387



Internal ID22521273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27013074..27013663hg38UCSC Ensembl
chrX:27031191..27031780hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38590
hg19590
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975096
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463387
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