A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998487



Internal ID21907830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:9357382..9376753hg38UCSC Ensembl
chr4:9359108..9378479hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3819372
hg1919372
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547988
Samples
Known GenesUSP17L24, USP17L25, USP17L26, USP17L27, USP17L28, USP17L29, USP17L30, USP17L5, USP17L6P, USP17L9P
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998487
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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