A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14354919



Internal ID22234787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154519722..154519820hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3899
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3525965
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14354919
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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