A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526332



Internal ID22395712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182153133..182153263hg38UCSC Ensembl
chr3:181870921..181871051hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14310143, nssv14310144
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526332
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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