A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111202



Internal ID21294468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:7767360..7773836hg38UCSC Ensembl
Innerchr1:7827420..7833896hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg386477
hg196477
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099141
Samplessample360
Known GenesCAMTA1, VAMP3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111202
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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