A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3231997



Internal ID22372390
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14351633, nssv14351632, nssv14351635, nssv14351634
SamplesHG00731, HG00733, HG00513, HG00514
Known GenesDMD
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3231997
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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