A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884944



Internal ID22659928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66986156..67009761hg38UCSC Ensembl
chr16:67020059..67043664hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3823606
hg1923606
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479048
Samples
Known GenesCES4A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884944
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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