A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391635



Internal ID21382665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:76134751..76134855hg38UCSC Ensembl
chr16:76168649..76168753hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15706075
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391635
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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