A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588632



Internal ID20961703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106058182..106058577hg38UCSC Ensembl
chr11:105928909..105929304hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1302n223
Supporting Variantsnssv18233049
Samples
Known GenesKBTBD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588632
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