A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112534



Internal ID21295800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:3755709..3762297hg38UCSC Ensembl
Innerchr6:3755943..3762531hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg386589
hg196589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086395
Samplessample138
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112534
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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