A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15748851



Internal ID21386608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88373593..88381592hg38UCSC Ensembl
chr16:88440001..88448000hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432404
Supporting Variants
SamplesMDQ025
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15748851
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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