A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028107



Internal ID21937450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63099104..63099159hg38UCSC Ensembl
chr15:63391303..63391358hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610644
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028107
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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