A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579359



Internal ID20952430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110153415..110154126hg38UCSC Ensembl
chr11:110024140..110024851hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38712
hg19712
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231603
Samples
Known GenesZC3H12C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579359
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