A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594148



Internal ID20967219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13395942..13396340hg38UCSC Ensembl
chr10:13437942..13438340hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222423
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594148
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