A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020779



Internal ID21930122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66260330..66260457hg38UCSC Ensembl
chr15:66552668..66552795hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601622
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020779
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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