A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012642



Internal ID21921985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139872728..139872928hg38UCSC Ensembl
chr8:140884972..140885172hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594440
Samples
Known GenesTRAPPC9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012642
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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