A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595606



Internal ID20968677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25581518..25582683hg38UCSC Ensembl
chr20:25562154..25563319hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg381166
hg191166
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4426n223
Supporting Variantsnssv18254316
Samples
Known GenesNINL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595606
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