A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410581



Internal ID21068134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20472527..20864716hg38UCSC Ensembl
chr6:20472758..20864947hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38392190
hg19392190
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236226
Samples
Known GenesCDKAL1, E2F3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410581
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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