A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560898



Internal ID22429693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3016165..3016165hg38UCSC Ensembl
chr18:3016163..3016163hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14284890, nssv14284887, nssv14284884, nssv14284883, nssv14284888, nssv14284885, nssv14284889, nssv14284886
SamplesHG00512, NA19238, NA19239, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560898
Frequency
Sample Size9
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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