A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115434



Internal ID21298700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:23220792..23231269hg38UCSC Ensembl
Innerchr1:23547285..23557762hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3810478
hg1910478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104697
Samplessample51
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115434
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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