A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539229



Internal ID20912533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:116895766..116896432hg38UCSC Ensembl
chr1:117438388..117439054hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg38667
hg19667
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249863
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539229
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