A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583479



Internal ID20956550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43320319..43320512hg38UCSC Ensembl
chr11:43341869..43342062hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234435
Samples
Known GenesAPI5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583479
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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