A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420403



Internal ID21077956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139902201..139990900hg38UCSC Ensembl
chr8:140914445..141001110hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3888700
hg1986666
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234767
Samples
Known GenesTRAPPC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420403
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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