A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17168640



Internal ID21512768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:76141864..76153243hg38UCSC Ensembl
chrX:75361699..75373078hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg3811380
hg1911380
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667892
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17168640
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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