A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877212



Internal ID22652175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:952761..995593hg38UCSC Ensembl
chr16:1002761..1045593hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3842833
hg1942833
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474840
Samples
Known GenesLMF1, SOX8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877212
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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