A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561413



Internal ID22430181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155991254..155991254hg38UCSC Ensembl
chr1:155961045..155961045hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14289158
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561413
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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