A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17117001



Internal ID21451463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56188986..56189162hg38UCSC Ensembl
chr20:54764042..54764218hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598265
Supporting Variants
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17117001
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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