A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432333



Internal ID21394335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26373680..26375679hg38UCSC Ensembl
chr16:26385001..26387000hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15751795, nssv15754356, nssv15747815
SamplesBTQ016, NB07, NB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432333
Frequency
Sample Size15
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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