A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114682



Internal ID21297948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:178592159..178594612hg38UCSC Ensembl
Innerchr3:178309947..178312400hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg382454
hg192454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14106371
Samplessample138
Known GenesKCNMB2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114682
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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