A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115753



Internal ID21299019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:87326447..87332182hg38UCSC Ensembl
Innerchr1:87792130..87797865hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg385736
hg195736
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv47n145
Supporting Variantsnssv14099948, nssv14088601
Samplessample404, sample263
Known GenesLMO4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115753
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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