A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742575



Internal ID166241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:137301381..137315381hg38UCSC Ensembl
chrX:136383540..136397540hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3814001
hg1914001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138227
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742575
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0025047


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