A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5430736



Internal ID209533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41300504..41303049hg38UCSC Ensembl
chrX:41159757..41162302hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg382546
hg192546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736564
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5430736
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