A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664680



Internal ID21612985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58831769..58831769hg38UCSC Ensembl
chr20:57406824..57406824hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117166
SamplesHG01596
Known GenesGNAS-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664680
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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