A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563561



Internal ID22432297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26316534..26316534hg38UCSC Ensembl
chr4:26318156..26318156hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14311959, nssv14311961, nssv14311960
SamplesHG00512, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563561
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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