A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414653



Internal ID21072206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:65432704..65455473hg38UCSC Ensembl
chr6:66142597..66165366hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3822770
hg1922770
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224747
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414653
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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