A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561682



Internal ID22430450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24219065..24219065hg38UCSC Ensembl
chr1:24545555..24545555hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14357386, nssv14357385
SamplesHG00732, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561682
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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