A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557900



Internal ID20930971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80220160..80221460hg38UCSC Ensembl
chr8:81132395..81133695hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg381301
hg191301
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278790
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557900
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