A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880899



Internal ID22655870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47175586..47187517hg38UCSC Ensembl
chr16:47209497..47221428hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3811932
hg1911932
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478989
Samples
Known GenesITFG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880899
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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