A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596369



Internal ID20969440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47084580..47085029hg38UCSC Ensembl
chr20:45713219..45713668hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252156
Samples
Known GenesEYA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596369
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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