A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561515



Internal ID22430283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:8516146..8516146hg38UCSC Ensembl
chr18:8516144..8516144hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14289752, nssv14289753
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561515
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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