A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14350691



Internal ID22207260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24258133..24258630hg38UCSC Ensembl
chrX:24276250..24276747hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3199137
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14350691
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