A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525332



Internal ID22394709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14308660..14308733hg38UCSC Ensembl
chr5:14308769..14308842hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7211n152
Supporting Variantsnssv14320330, nssv14320331
SamplesNA19239, NA19240
Known GenesTRIO
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525332
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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