A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562391



Internal ID20935462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:15859520..15862411hg38UCSC Ensembl
chr5:15859629..15862520hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg382892
hg192892
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267405
Samples
Known GenesFBXL7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562391
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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