A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118030



Internal ID21301296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:25087917..25103422hg38UCSC Ensembl
Innerchr7:25127536..25143041hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3815506
hg1915506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086810
Samplessample359
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118030
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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