A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220422



Internal ID22365120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20828565..20828633hg38UCSC Ensembl
chr14:21296724..21296792hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14372464
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220422
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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