A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525361



Internal ID22394739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45721206..45721262hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10104n152
Supporting Variantsnssv14351081, nssv14351080, nssv14351083, nssv14351082, nssv14351084
SamplesHG00512, NA19238, NA19240, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525361
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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