A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741812



Internal ID165478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:106036616..106055924hg38UCSC Ensembl
chrX:105280607..105299915hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3819309
hg1919309
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421403
Supporting Variants
Samples
Known GenesSERPINA7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741812
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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