A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3562638



Internal ID22431384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139780460..139780460hg38UCSC Ensembl
chr3:139499302..139499302hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14309504
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3562638
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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