A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884411



Internal ID22659393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:68476187..68476488hg38UCSC Ensembl
chrX:67696029..67696330hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464689
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884411
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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