A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086020



Internal ID21452170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45144396..45144595hg38UCSC Ensembl
chr17:43221763..43221962hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587211
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086020
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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