A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557976



Internal ID331053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:51510587..51539849hg38UCSC Ensembl
chrX:51253439..51282701hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3829263
hg1929263
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557976
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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