A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432372



Internal ID21394374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:78137769..78138447hg38UCSC Ensembl
chr16:78171666..78172344hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38679
hg19679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15752421, nssv15746554
SamplesNB08, NB09
Known GenesWWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432372
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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