A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202732



Internal ID22351851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105994629..105995953hg38UCSC Ensembl
chr6:106442504..106443828hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381325
hg191325
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14330698, nssv14330703, nssv14330699, nssv14330700, nssv14330695, nssv14330701, nssv14330702, nssv14330697, nssv14330696
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)nsv3202732
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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