A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17548859



Internal ID21873214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118901911..118902024hg38UCSC Ensembl
chr4:119823066..119823179hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5994874
Supporting Variants
Samples
Known GenesSYNPO2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17548859
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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