A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052334



Internal ID21961568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:43953793..43953793hg38UCSC Ensembl
chr2:44180932..44180932hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530800
Samples
Known GenesLRPPRC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052334
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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