A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5986665



Internal ID21896008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:140426778..140432386hg38UCSC Ensembl
chr2:141184347..141189955hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg385609
hg195609
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518060
Samples
Known GenesLRP1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5986665
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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