A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432393



Internal ID21394395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8661421..8662996hg38UCSC Ensembl
chr16:8755278..8756853hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg381576
hg191576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15751354
SamplesSMI041
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432393
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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