A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17126314



Internal ID21478523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1857815..1857815hg38UCSC Ensembl
chr5:1857929..1857929hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5628379
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17126314
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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