A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14357675



Internal ID22182537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35222309..35237978hg38UCSC Ensembl
chr11:35243856..35259525hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3815670
hg1915670
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3220536
Supporting Variants
SamplesHG00514
Known GenesCD44
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14357675
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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