A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434953



Internal ID22492823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:125098742..125100294hg38UCSC Ensembl
chrX:124232591..124234143hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg381553
hg191553
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976492
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434953
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