A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052874



Internal ID21962107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:45415171..45415171hg38UCSC Ensembl
chr2:45642310..45642310hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17521946
Samples
Known GenesSRBD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052874
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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