A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553680



Internal ID20926791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:53904727..53905239hg38UCSC Ensembl
chr2:54131864..54132376hg19UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258180
Samples
Known GenesPSME4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553680
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