A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593777



Internal ID20966848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118863208..118863731hg38UCSC Ensembl
chr11:118733917..118734440hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1322n223
Supporting Variantsnssv18227280
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593777
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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