A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14352132



Internal ID22162828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:68953105..68953207hg38UCSC Ensembl
chrX:68172948..68173050hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3199103
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14352132
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