A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15747815



Internal ID21388275
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 StatusS
Merged Variantsnsv4432333
Supporting Variants
SamplesNB07
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15747815
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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