A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105283



Internal ID22014516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:86834564..86835431hg38UCSC Ensembl
chrX:86089567..86090434hg19UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg38868
hg19868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641596
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105283
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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