A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15748828



Internal ID21390744
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 StatusS
Merged Variantsnsv4432311
Supporting Variants
SamplesNB11
Known GenesUNKL
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15748828
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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