A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3562820



Internal ID22431564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27167749..27167749hg38UCSC Ensembl
chr2:27390617..27390617hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14292057, nssv14292058
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3562820
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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