A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555483



Internal ID20928570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63170306..63170650hg38UCSC Ensembl
chr1:63635977..63636321hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250569
Samples
Known GenesLINC00466
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555483
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