A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3246889



Internal ID22376559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96866677..96871890hg38UCSC Ensembl
chr15:97409907..97415120hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg385214
hg195214
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14379737, nssv14381162, nssv14384887, nssv14374497, nssv14378296, nssv14392410, nssv14377876, nssv14383304
SamplesHG00512, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3246889
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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