A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14291284



Internal ID22222121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:120823235..120959883hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38136649
Variant TypeCNV duplication
Copy Number73
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206454
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14291284
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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