A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595189



Internal ID20968260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58681359..58682573hg38UCSC Ensembl
chr10:60441119..60442333hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg381215
hg191215
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236326
Samples
Known GenesBICC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595189
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