A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118232



Internal ID21301498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:92956228..93066135hg38UCSC Ensembl
Innerchr4:93877379..93987286hg19UCSC Ensembl
Cytoband4q22.2
Allele length
AssemblyAllele length
hg38109908
hg19109908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv906n145
Supporting Variantsnssv14090665, nssv14090723
Samplessample178, sample188
Known GenesGRID2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118232
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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