A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545298



Internal ID20918528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52646842..52647879hg38UCSC Ensembl
chr1:53112514..53113551hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg381038
hg191038
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249738
Samples
Known GenesFAM159A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545298
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer