A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668677



Internal ID21616982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102317110..102348484hg38UCSC Ensembl
chrX:101572067..101603407hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3831375
hg1931341
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165003
SamplesHG00732
Known GenesNXF2, NXF2B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668677
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