A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088494



Internal ID21997727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64067284..64067284hg38UCSC Ensembl
chr15:64359483..64359483hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610988
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088494
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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