A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539080



Internal ID20912387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:197642708..197643385hg38UCSC Ensembl
chr2:198507432..198508109hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38678
hg19678
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257122
Samples
Known GenesRFTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539080
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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