A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046883



Internal ID21956116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15463236..15463236hg38UCSC Ensembl
chr1:15789731..15789731hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536852
Samples
Known GenesCELA2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046883
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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