A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583794



Internal ID20956865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107456376..107502750hg38UCSC Ensembl
chr13:108108724..108155098hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3846375
hg1946375
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230616
Samples
Known GenesFAM155A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583794
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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