A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884470



Internal ID22659453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20793119..20794768hg38UCSC Ensembl
chr16:20804441..20806090hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg381650
hg191650
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477594
Samples
Known GenesACSM3, ERI2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884470
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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