A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413783



Internal ID21071336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42233435..42234487hg38UCSC Ensembl
chr6:42201173..42202225hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381053
hg191053
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143366
Samples
Known GenesTRERF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413783
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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