A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561873



Internal ID22430641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35226721..35226721hg38UCSC Ensembl
chr20:33814524..33814524hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14299948, nssv14299956, nssv14299955, nssv14299954, nssv14299952, nssv14299951, nssv14299950, nssv14299949, nssv14299953
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)nsv3561873
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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