A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14351869



Internal ID22139644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:58539767..58555579hg38UCSC Ensembl
chrX:58566200..58582012hg19UCSC Ensembl
CytobandXp11.1
Allele length
AssemblyAllele length
hg3815813
hg1915813
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3210286
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14351869
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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