A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083206



Internal ID21290502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:139196558..139212473hg38UCSC Ensembl
Innerchr7:138881304..138897219hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3815916
hg1915916
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116036
Supporting Variants
Samplessample60
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083206
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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