A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736311



Internal ID159977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27883158..27889750hg38UCSC Ensembl
chrX:27901275..27907867hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg386593
hg196593
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431858
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736311
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00312175


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