A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113653



Internal ID21296919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:88660190..88666750hg38UCSC Ensembl
Innerchr3:88709340..88715900hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg386561
hg196561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv772n145
Supporting Variantsnssv14107811
Samplessample280
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113653
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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