A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739067



Internal ID162733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6509592..6801695hg38UCSC Ensembl
chrX:6427633..6719736hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38292104
hg19292104
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5418161
Supporting Variants
Samples
Known GenesVCX3A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739067
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