A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594724



Internal ID20967795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45981196..45982141hg38UCSC Ensembl
chr11:46002747..46003692hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38946
hg19946
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219509
Samples
Known GenesPHF21A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594724
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