A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599858



Internal ID20972929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29739958..29742352hg38UCSC Ensembl
chr22:30135947..30138341hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg382395
hg192395
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255500
Samples
Known GenesZMAT5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599858
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