A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563220



Internal ID22431960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13154460..13154460hg38UCSC Ensembl
chr3:13195960..13195960hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14305356, nssv14305355, nssv14305354
SamplesHG00512, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563220
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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