A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5421153



Internal ID200237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:145312343..145312945hg38UCSC Ensembl
chrX:144393862..144394464hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38603
hg19603
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737751
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5421153
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