A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415490



Internal ID21073043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63871796..64089587hg38UCSC Ensembl
chr6:64581689..64799480hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38217792
hg19217792
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235485
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415490
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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