A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5986297



Internal ID21895640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:141580687..141662017hg38UCSC Ensembl
chr2:142338256..142419586hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg3881331
hg1981331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530251
Samples
Known GenesLRP1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5986297
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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