A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560589



Internal ID22429387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83176939..83176939hg38UCSC Ensembl
chr15:83845691..83845691hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14387983, nssv14382328, nssv14384974, nssv14390091, nssv14386200, nssv14389206
SamplesNA19238, NA19239, HG00732, NA19240, HG00733, HG00513
Known GenesHDGFRP3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560589
Frequency
Sample Size9
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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