A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391659



Internal ID21382689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87693664..87693735hg38UCSC Ensembl
chr16:87727270..87727341hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15706090
Samples
Known GenesJPH3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391659
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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