A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525327



Internal ID22394704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:109212586..109212703hg38UCSC Ensembl
chrX:108455815..108455932hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10232n152
Supporting Variantsnssv14353865, nssv14353866, nssv14353867, nssv14353863, nssv14353864
SamplesHG00512, HG00732, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525327
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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