A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110838



Internal ID21294104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:74172653..74176045hg38UCSC Ensembl
Innerchr7:73586983..73590375hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg383393
hg193393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086780
Samplessample349
Known GenesEIF4H
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110838
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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