A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588131



Internal ID20961202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102129527..102129873hg38UCSC Ensembl
chr11:102000258..102000604hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1294n223
Supporting Variantsnssv18230467
Samples
Known GenesYAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588131
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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