A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113442



Internal ID21296708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22372516..23119040hg38UCSC Ensembl
Innerchr15:22754028..23500580hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38746525
hg19746553
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096139
Samplessample137
Known GenesCYFIP1, GOLGA8EP, GOLGA8I, HERC2P2, HERC2P7, LOC283683, NIPA1, NIPA2, TUBGCP5, WHAMMP3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113442
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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