A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969465



Internal ID22744400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:95053975..95063485hg38UCSC Ensembl
chrX:94308974..94318484hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg389511
hg199511
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969465
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