A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528360



Internal ID22397747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18333067..18333148hg38UCSC Ensembl
chrUn_gl000212:161819..161900hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14366061
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528360
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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