A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111280



Internal ID21294546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:28412684..28426335hg38UCSC Ensembl
Innerchr3:28454175..28467826hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3813652
hg1913652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108125
Samplessample202
Known GenesZCWPW2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111280
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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