A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113605



Internal ID21296871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:128695367..128703891hg38UCSC Ensembl
Innerchr7:128335421..128343945hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg388525
hg198525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14084854
Samplessample48
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113605
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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