A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116514



Internal ID21299780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:72519839..72539361hg38UCSC Ensembl
Innerchr7:71984824..72004346hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3819523
hg1919523
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14083272
Samplessample76
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116514
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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