A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3530071



Internal ID22399462
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14358116, nssv14358118, nssv14358117, nssv14358122, nssv14358119, nssv14358123, nssv14358121, nssv14358120
SamplesHG00512, NA19238, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesOLFML1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3530071
Frequency
Sample Size9
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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