A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535763



Internal ID20909116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:47866281..47866410hg38UCSC Ensembl
chr2:48093420..48093549hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258067
Samples
Known GenesFBXO11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535763
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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