A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434017



Internal ID22491887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102143122..102143651hg38UCSC Ensembl
chrX:101398094..101398623hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38530
hg19530
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970841
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434017
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