A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114711



Internal ID21297977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:169261419..169269543hg38UCSC Ensembl
Innerchr1:169230657..169238781hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg388125
hg198125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093250
Samplessample285
Known GenesNME7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114711
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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