A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451281



Internal ID21108834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6729536..6788843hg38UCSC Ensembl
chr11:6750767..6810074hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3859308
hg1959308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993482
Samples
Known GenesOR2AG1, OR2AG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451281
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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