A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459453



Internal ID21117006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124225572..124265772hg38UCSC Ensembl
chr11:124096278..124135668hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3840201
hg1939391
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180097
Samples
Known GenesOR8G1, OR8G2, OR8G5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459453
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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