A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14351006



Internal ID22263273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3691430..3691485hg38UCSC Ensembl
chrX:3609471..3609526hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3526965
Supporting Variants
SamplesNA19238
Known GenesPRKX
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14351006
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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