A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564773



Internal ID20937844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:65476903..66457398hg38UCSC Ensembl
chr6:66186796..67167291hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38980496
hg19980496
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273941
Samples
Known GenesEYS, SLC25A51P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564773
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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