A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573783



Internal ID20946854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13014836..13015592hg38UCSC Ensembl
chr8:12872345..12873101hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38757
hg19757
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276260
Samples
Known GenesKIAA1456
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573783
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