A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3562958



Internal ID22431700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150135402..150135402hg38UCSC Ensembl
chr3:149853189..149853189hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14308266, nssv14308270, nssv14308268, nssv14308263, nssv14308264, nssv14308269, nssv14308265, nssv14308267, nssv14308262
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3562958
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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