A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097820



Internal ID21284788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:25278187..25282793hg38UCSC Ensembl
Innerchr16:25289508..25294114hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg384607
hg194607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117420
Supporting Variants
Samplessample365
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097820
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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