A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597832



Internal ID20970903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:558351..1188654hg38UCSC Ensembl
chr19:558351..1188653hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38630304
hg19630303
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248493
Samples
Known GenesABCA7, ARID3A, AZU1, BSG, CFD, CNN2, ELANE, FGF22, FSTL3, GPX4, GRIN3B, HCN2, HMHA1, KISS1R, LPPR3, MED16, MIR3187, MIR4745, MISP, PALM, POLR2E, POLRMT, PRSS57, PRTN3, PTBP1, R3HDM4, RNF126, SBNO2, TMEM259, WDR18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597832
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