A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112655



Internal ID22021888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2652733..2652733hg38UCSC Ensembl
chr20:2633379..2633379hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632676
Samples
Known GenesNOP56
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112655
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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