A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741405



Internal ID165071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:90773617..90773808hg38UCSC Ensembl
chrX:90028616..90028807hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554429
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741405
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.169216


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