A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560906



Internal ID22429701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:41596782..41596782hg38UCSC Ensembl
chr18:39176746..39176746hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14283928, nssv14283929, nssv14283927
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560906
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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