A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870369



Internal ID22645305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23204772..23205971hg38UCSC Ensembl
chr16:23216093..23217292hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477667
Samples
Known GenesSCNN1G
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870369
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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