A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561495



Internal ID334474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:91471822..91471873hg38UCSC Ensembl
chrX:90726821..90726872hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38253
hg19253
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741429
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561495
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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