A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214419



Internal ID22361084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107388994..107390016hg38UCSC Ensembl
chr9:110151275..110152297hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381023
hg191023
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14348260, nssv14348262, nssv14348265, nssv14348259, nssv14348261, nssv14348264, nssv14348258, nssv14348266, nssv14348263
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)nsv3214419
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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