A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084378



Internal ID21993611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53329861..53329861hg38UCSC Ensembl
chr15:53622058..53622058hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609397
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084378
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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