A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739433



Internal ID163099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:16522221..16535008hg38UCSC Ensembl
chrX:16540344..16553131hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3812788
hg1912788
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426601
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739433
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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