A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5416071



Internal ID195311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102338656..102349000hg38UCSC Ensembl
chrX:101593579..101603923hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3810345
hg1910345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741755
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5416071
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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