A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17528719



Internal ID21853076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:45414995..45414995hg38UCSC Ensembl
chr2:45642134..45642134hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6056401
Supporting Variants
Samples
Known GenesSRBD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17528719
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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