A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413306



Internal ID21070859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:18259339..18260910hg38UCSC Ensembl
chr6:18259570..18261141hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381572
hg191572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143049
Samples
Known GenesDEK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413306
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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