A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559035



Internal ID20932106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28144580..28145915hg38UCSC Ensembl
chr8:28002097..28003432hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg381336
hg191336
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277598
Samples
Known GenesELP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559035
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