A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117822



Internal ID21301088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:29761203..29762982hg38UCSC Ensembl
Innerchr3:29802694..29804473hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg381780
hg191780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14107738, nssv14107024, nssv14105579
Samplessample252, sample270, sample418
Known GenesRBMS3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117822
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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