A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17117778



Internal ID21410521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63880003..63880122hg38UCSC Ensembl
chr20:62511356..62511475hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5585916
Supporting Variants
SamplesHG00513
Known GenesTPD52L2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17117778
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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