A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761695



Internal ID20537555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46951386..46971306hg38UCSC Ensembl
chrX:46810661..46830781hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3819921
hg1920121
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296222
Samples
Known GenesJADE3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761695
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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