A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17530251



Internal ID21854607
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 StatusS
Merged Variantsnsv5986297
Supporting Variants
Samples
Known GenesLRP1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17530251
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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