A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3946514



Internal ID21366583
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 Variantsnssv15199658
SamplesHG002
Known GenesTRAPPC9
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3946514
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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