A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116487



Internal ID21299753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:41930593..41936016hg38UCSC Ensembl
Innerchr7:41970191..41975614hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg385424
hg195424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14084250
Samplessample140
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116487
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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