A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043502



Internal ID21952796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:45415090..45415090hg38UCSC Ensembl
chr2:45642229..45642229hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17532603
Samples
Known GenesSRBD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043502
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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