A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592051



Internal ID20965122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:48357187..50028180hg38UCSC Ensembl
chr11:48378739..50039360hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg381670994
hg191660622
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1040n223
Supporting Variantsnssv18228394
Samples
Known GenesFOLH1, LOC440040, OR4A47, OR4C12, OR4C13, TRIM49B, TRIM64C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592051
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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