A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554474



Internal ID20927568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149946626..149948197hg38UCSC Ensembl
chr1:149918526..149920098hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg381572
hg191573
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247505
Samples
Known GenesOTUD7B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554474
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