A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220960



Internal ID22365501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41031621..41040138hg38UCSC Ensembl
chr15:41323819..41332336hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg388518
hg198518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14392069
SamplesNA19240
Known GenesINO80
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220960
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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