A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116060



Internal ID21299326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:115412519..115432487hg38UCSC Ensembl
Innerchr7:115052573..115072541hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3819969
hg1919969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086727
Samplessample339
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116060
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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