A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421413



Internal ID21078966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:103425801..103427300hg38UCSC Ensembl
chr8:104438029..104439528hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162625
Samples
Known GenesDCAF13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421413
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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