A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115190



Internal ID21298456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:35267531..35270021hg38UCSC Ensembl
Innerchr1:35733132..35735622hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg382491
hg192491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096619
Samplessample136
Known GenesZMYM4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115190
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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