A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737206



Internal ID160872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:116927845..116961973hg38UCSC Ensembl
chrX:116061813..116095941hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3834129
hg1934129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420243
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737206
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0024974


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