A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004216



Internal ID21913559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42758059..42766218hg38UCSC Ensembl
chr8:42613202..42621361hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg388160
hg198160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585048
Samples
Known GenesCHRNA6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004216
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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