A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14351632



Internal ID22139496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:32065974..32075658hg38UCSC Ensembl
chrX:32084091..32093775hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg389685
hg199685
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3231997
Supporting Variants
SamplesHG00513
Known GenesDMD
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14351632
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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