A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575537



Internal ID20948608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58654412..58654929hg38UCSC Ensembl
chr8:59566971..59567488hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38518
hg19518
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278341
Samples
Known GenesNSMAF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575537
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