A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3212712



Internal ID22359878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92767811..92769752hg38UCSC Ensembl
chr15:93311041..93312982hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381942
hg191942
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3027n152
Supporting Variantsnssv14374201, nssv14387191, nssv14380686, nssv14372937, nssv14391822
SamplesNA19238, NA19239, HG00732, NA19240, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3212712
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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