A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537170



Internal ID20910510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:239077272..239080040hg38UCSC Ensembl
chr1:239240572..239243340hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg382769
hg192769
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250075
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537170
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