A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593304



Internal ID20966375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:48341202..50038018hg38UCSC Ensembl
chr11:48362754..50039360hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg381696817
hg191676607
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1040n223
Supporting Variantsnssv18224174
Samples
Known GenesFOLH1, LOC440040, OR4A47, OR4C12, OR4C13, OR4C45, TRIM49B, TRIM64C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593304
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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