A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115946



Internal ID21299212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:94255666..94279755hg38UCSC Ensembl
Innerchr7:93884978..93909067hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3824090
hg1924090
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14084318
Samplessample150
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115946
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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