A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871363



Internal ID22646301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57276000..57277799hg38UCSC Ensembl
chr16:57309912..57311711hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479016
Samples
Known GenesPLLP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871363
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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