A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14351928



Internal ID22284654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:65894119..65894573hg38UCSC Ensembl
chrX:65113961..65114415hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3525968
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14351928
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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