A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220771



Internal ID22365375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65254367..65254647hg38UCSC Ensembl
chr14:65721085..65721365hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14370365
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220771
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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