A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14342195



Internal ID22210036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102529884..102536104hg38UCSC Ensembl
chr8:103542112..103548332hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg386221
hg196221
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3224524
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14342195
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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