A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224335



Internal ID20791375
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 StatusS
Merged Variantsnsv6404208
Supporting Variants
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224335
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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