A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14353576



Internal ID22233681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:129858931..129859730hg38UCSC Ensembl
chrX:128992907..128993706hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3234285
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14353576
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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