A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665484



Internal ID21613789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103954976..104083087hg38UCSC Ensembl
chrX:103209549..103324337hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg38128112
hg19114789
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165185
Samples
Known GenesH2BFM, H2BFWT, H2BFXP, MIR1256, TMSB15B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665484
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