A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116579



Internal ID21404779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43696733..43696733hg38UCSC Ensembl
chr20:42325373..42325373hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38505
hg19505
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664585
Supporting Variants
SamplesHG00512
Known GenesMYBL2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116579
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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