A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410107



Internal ID21067660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:65611801..65640300hg38UCSC Ensembl
chr6:66321694..66350193hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3828500
hg1928500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229922
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410107
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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