A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573816



Internal ID20946887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42991415..42992632hg38UCSC Ensembl
chr8:42846558..42847775hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg381218
hg191218
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278075
Samples
Known GenesHOOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573816
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