A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3216440



Internal ID22362432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156941435..156941945hg38UCSC Ensembl
chr7:156734129..156734639hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38511
hg19511
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14338855, nssv14338857, nssv14338856
SamplesHG00512, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3216440
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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