A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17137658



Internal ID21401119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184697354..184697425hg38UCSC Ensembl
chr4:185618508..185618579hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582441
Supporting Variants
SamplesHG00096
Known GenesCENPU
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17137658
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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