A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736138



Internal ID159804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3817000..3847000hg38UCSC Ensembl
chrX:3735041..3765041hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3830001
hg1930001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138063
Supporting Variants
Samples
Known GenesLOC389906
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736138
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00139925


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