A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561451



Internal ID22430219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:213791000..213791000hg38UCSC Ensembl
chr1:213964343..213964343hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14307678, nssv14307676, nssv14307677, nssv14307675
SamplesNA19238, NA19239, HG00732, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561451
Frequency
Sample Size9
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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