A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114666



Internal ID21297932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:61750028..61753580hg38UCSC Ensembl
Innerchr4:62615746..62619298hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg383553
hg193553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14107603
Samplessample84
Known GenesLPHN3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114666
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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