A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576377



Internal ID20949448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9892129..9894517hg38UCSC Ensembl
chr11:9913676..9916064hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382389
hg192389
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218950
Samples
Known GenesSBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576377
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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