A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5423735



Internal ID202747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149090682..149090865hg38UCSC Ensembl
chrX:148172212..148172395hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737896
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5423735
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