A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560998



Internal ID22429792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24521939..24521939hg38UCSC Ensembl
chr18:22101903..22101903hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14290858, nssv14290860, nssv14290859
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560998
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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