A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14353863



Internal ID22126862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:109212586..109212703hg38UCSC Ensembl
chrX:108455815..108455932hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3525327
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14353863
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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