A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112479



Internal ID21295745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:3714670..3721829hg38UCSC Ensembl
Innerchr6:3714904..3722063hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg387160
hg197160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14083002
Samplessample333
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112479
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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