A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14299285



Internal ID22162825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9855838..9859914hg38UCSC Ensembl
chr4_gl000193_random:123152..127228hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg384077
hg194077
Variant TypeCNV duplication
Copy Number6
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3213564
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14299285
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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