A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561047



Internal ID22429840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66864649..66864649hg38UCSC Ensembl
chr15:67156987..67156987hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14376036, nssv14376271, nssv14383092, nssv14379277, nssv14383778
SamplesNA19238, NA19239, NA19240, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561047
Frequency
Sample Size9
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer