A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600022



Internal ID20973093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6297054..6330111hg38UCSC Ensembl
chr19:6297065..6330122hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3833058
hg1933058
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249152
Samples
Known GenesACER1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600022
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