A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755573



Internal ID20531433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:22818689..22818689hg38UCSC Ensembl
chr16:22830010..22830010hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284941
Samples
Known GenesHS3ST2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755573
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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