A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566633



Internal ID20939704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:37343329..37343616hg38UCSC Ensembl
chr5:37343431..37343718hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268883
Samples
Known GenesNUP155
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566633
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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