A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583700



Internal ID20956771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:20061464..20062863hg38UCSC Ensembl
chr11:20083010..20084409hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233445
Samples
Known GenesNAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583700
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