A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018799



Internal ID21928142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166396261..166396345hg38UCSC Ensembl
chr6:166809749..166809833hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575518
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018799
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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