A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561002



Internal ID22429796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34742629..34742629hg38UCSC Ensembl
chr18:32322593..32322593hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14283356, nssv14283355
SamplesHG00513, HG00514
Known GenesDTNA
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561002
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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