A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14361375



Internal ID22212504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120920679..120920771hg38UCSC Ensembl
chr11:120791388..120791480hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3220530
Supporting Variants
SamplesHG00733
Known GenesGRIK4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14361375
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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