A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116326



Internal ID21458679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3083082..3083082hg38UCSC Ensembl
chr20:3063728..3063728hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38506
hg19506
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651728
Supporting Variants
SamplesHG02587
Known GenesAVP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116326
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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