A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555902



Internal ID20928973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36251167..36251897hg38UCSC Ensembl
chr6:36218944..36219674hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270705
Samples
Known GenesPNPLA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555902
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