A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115390



Internal ID21298656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:121419397..121443118hg38UCSC Ensembl
Innerchr7:121059451..121083172hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3823722
hg1923722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086695
Samplessample332
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115390
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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