A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432311



Internal ID21394313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1397367..1397755hg38UCSC Ensembl
chr16:1447368..1447756hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv275n172
Supporting Variantsnssv15748828
SamplesNB11
Known GenesUNKL
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432311
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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