A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118273



Internal ID21301539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161711592..161735886hg38UCSC Ensembl
Innerchr1:161681382..161705676hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3824295
hg1924295
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099384
Samplessample378
Known GenesFCRLA, FCRLB
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118273
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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