A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106720



Internal ID22015954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1603639..1603639hg38UCSC Ensembl
chr20:1584285..1584285hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630617
Samples
Known GenesSIRPB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106720
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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