A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110463



Internal ID21293729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140305935..140309077hg38UCSC Ensembl
Innerchr7:140005735..140008877hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg383143
hg193143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086877, nssv14084276, nssv14084771, nssv14086829, nssv14084579, nssv14084841
Samplessample373, sample205, sample143, sample32, sample362, sample46
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110463
Frequency
Sample Size467
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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