A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101225



Internal ID22010458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:84811267..84820839hg38UCSC Ensembl
chrX:84066274..84075846hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg389573
hg199573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643068
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101225
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