A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884387



Internal ID22659369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47181912..47186618hg38UCSC Ensembl
chr16:47215823..47220529hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg384707
hg194707
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv841n209
Supporting Variantsnssv17471549
Samples
Known GenesITFG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884387
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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