A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116441



Internal ID21299707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143728212..143847008hg38UCSC Ensembl
Innerchr7:143425305..143544101hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38118797
hg19118797
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14084279
Samplessample143
Known GenesCTAGE6, FAM115C, LOC154761
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116441
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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