A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980297



Internal ID22755232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:56053856..56063800hg38UCSC Ensembl
chrX:56080289..56090233hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg389945
hg199945
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516393
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5980297
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