A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3217232



Internal ID22362957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110509459..110510632hg38UCSC Ensembl
chr10:112269217..112270390hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg381174
hg191174
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14354453, nssv14354457, nssv14354455, nssv14354450, nssv14354454, nssv14354456, nssv14354452, nssv14354451, nssv14354458
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesDUSP5
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3217232
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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