A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14353969



Internal ID22140912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115403403..115403623hg38UCSC Ensembl
chrX:114637977..114638347hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38221
hg19371
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3205728
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14353969
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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