A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555774



Internal ID328924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27655123..27655123hg38UCSC Ensembl
chrX:27673240..27673240hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg385871
hg195871
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736300
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555774
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