A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563024



Internal ID22431766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39247470..39247470hg38UCSC Ensembl
chr3:39288961..39288961hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14306033, nssv14306031, nssv14306030, nssv14306032
SamplesNA19238, NA19239, HG00731, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563024
Frequency
Sample Size9
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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