A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560440



Internal ID22429236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25871686..25871686hg38UCSC Ensembl
chr15:26116833..26116833hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14387170, nssv14377974
SamplesNA19238, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560440
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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