A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565079



Internal ID20938150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:68999755..69000337hg38UCSC Ensembl
chr8:69911990..69912572hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278573
Samples
Known GenesLOC100505718
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565079
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