A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3212041



Internal ID22359410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68691161..68691624hg38UCSC Ensembl
chr15:68983500..68983963hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14382186, nssv14374651, nssv14392145, nssv14377077, nssv14382627, nssv14390527, nssv14383787
SamplesHG00512, NA19239, HG00731, HG00732, NA19240, HG00513, HG00514
Known GenesCORO2B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3212041
Frequency
Sample Size9
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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