A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219701



Internal ID22364642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:46304920..46304971hg38UCSC Ensembl
chr15:46597118..46597169hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14378655, nssv14387457
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219701
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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