A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879108



Internal ID22654076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14184932..14199115hg38UCSC Ensembl
chr16:14278789..14292972hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3814184
hg1914184
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476259
Samples
Known GenesMKL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879108
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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