A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575803



Internal ID20948874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69150596..69150988hg38UCSC Ensembl
chr10:70910352..70910744hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38393
hg19393
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv799n223
Supporting Variantsnssv18230966
Samples
Known GenesVPS26A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575803
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