A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113664



Internal ID21296930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:121521661..121539212hg38UCSC Ensembl
Innerchr7:121161715..121179266hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3817552
hg1917552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14084649, nssv14085362
Samplessample219, sample238
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113664
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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