A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431352



Internal ID21088905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144234119..144267165hg38UCSC Ensembl
chr8:145289022..145322068hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3833047
hg1933047
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217825
Samples
Known GenesMIR7112-2, MROH1, SCXA, SCXB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431352
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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