A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213974



Internal ID22360756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72005955..72008732hg38UCSC Ensembl
chr10:73765713..73768490hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382778
hg192778
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14352791, nssv14352790, nssv14353413, nssv14353415, nssv14353416, nssv14353412, nssv14353414, nssv14353417, nssv14353411
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesCHST3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213974
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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