A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544693



Internal ID21869048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:23199344..23199344hg38UCSC Ensembl
chr4:23200967..23200967hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6072118
Supporting Variants
Samples
Known GenesMIR548AJ2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544693
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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