A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432343



Internal ID21394345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:49945256..49945799hg38UCSC Ensembl
chr16:49979167..49979710hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38544
hg19544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15747316
SamplesNB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432343
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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