A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14358123



Internal ID22324069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7491543..7491765hg38UCSC Ensembl
chr11:7512774..7512996hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3530071
Supporting Variants
SamplesNA19240
Known GenesOLFML1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14358123
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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