A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555170



Internal ID20928260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:231392060..231394362hg38UCSC Ensembl
chr1:231527806..231530108hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg382303
hg192303
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250364
Samples
Known GenesEGLN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555170
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