A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14359747



Internal ID22197169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62143053..62143212hg38UCSC Ensembl
chr11:61910525..61910684hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529373
Supporting Variants
SamplesHG00731
Known GenesINCENP
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14359747
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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