A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17139592



Internal ID21449655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:114500482..114659978hg38UCSC Ensembl
chr5:113836179..113995675hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg38159497
hg19159497
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572394
Supporting Variants
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17139592
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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