A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879005



Internal ID22653972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3054919..3072614hg38UCSC Ensembl
chr16:3104920..3122615hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3817696
hg1917696
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469899
Samples
Known GenesIL32, MMP25
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879005
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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