A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526387



Internal ID22395768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54065193..54065701hg38UCSC Ensembl
chrX:54091626..54092134hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38509
hg19509
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10129n152
Supporting Variantsnssv14351250, nssv14351253, nssv14351252, nssv14351251, nssv14351248, nssv14351249, nssv14351255, nssv14351254
SamplesHG00512, NA19238, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526387
Frequency
Sample Size9
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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