A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592554



Internal ID20965625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56114166..56468102hg38UCSC Ensembl
chr11:55881642..56235578hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38353937
hg19353937
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221932
Samples
Known GenesOR5J2, OR5M9, OR5R1, OR5T1, OR5T2, OR5T3, OR8H1, OR8H3, OR8J1, OR8J3, OR8K1, OR8K3, OR8K5, OR8U1, OR8U8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592554
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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