A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135259



Internal ID21416886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108690880..108690880hg38UCSC Ensembl
chr5:108026581..108026581hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5631042
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135259
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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