A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671676



Internal ID21619982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:52960473..52960473hg38UCSC Ensembl
chr20:51577012..51577012hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116616
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671676
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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