A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592012



Internal ID20965083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112887691..112888670hg38UCSC Ensembl
chr10:114647450..114648429hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38980
hg19980
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219084
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592012
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