A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452464



Internal ID21110017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6803560..6885434hg38UCSC Ensembl
chr11:6824791..6906665hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3881875
hg1981875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993541
Samples
Known GenesOR10A2, OR10A4, OR10A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452464
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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