A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553732



Internal ID20926844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153050617..153050806hg38UCSC Ensembl
chr1:153023093..153023282hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247043
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553732
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