A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404208



Internal ID21061761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63808295..63811121hg38UCSC Ensembl
chr6:64518188..64521014hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg382827
hg192827
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224335
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404208
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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