A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544568



Internal ID21868923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4526884..4526884hg38UCSC Ensembl
chr4:4528611..4528611hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6079148
Supporting Variants
Samples
Known GenesSTX18
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544568
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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