A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468368



Internal ID21125921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75280015..75280296hg38UCSC Ensembl
chr11:74991059..74991340hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993639
Samples
Known GenesARRB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468368
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer