A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593772



Internal ID20966843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70215038..70215677hg38UCSC Ensembl
chr10:71974794..71975433hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38640
hg19640
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224143
Samples
Known GenesPPA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593772
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