A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15706066



Internal ID21378342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66789291..66789624hg38UCSC Ensembl
chr16:66823194..66823527hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4391618
Supporting Variants
Samples
Known GenesCCDC79
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15706066
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.704023


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