A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14359331



Internal ID22143208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32470746..32476346hg38UCSC Ensembl
chr1:32936347..32941947hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg385601
hg195601
Variant TypeCNV duplication
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3199172
Supporting Variants
SamplesHG00513
Known GenesZBTB8B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14359331
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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