A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116401



Internal ID21299667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:57449928..57452855hg38UCSC Ensembl
Innerchr3:57435655..57438582hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg382928
hg192928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14103445
Samplessample15
Known GenesDNAH12
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116401
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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