A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591083



Internal ID20964154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12181807..12182775hg38UCSC Ensembl
chr10:12223806..12224774hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38969
hg19969
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv612n223
Supporting Variantsnssv18229824
Samples
Known GenesNUDT5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591083
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