A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594184



Internal ID20967255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9602315..9602998hg38UCSC Ensembl
chr11:9623862..9624545hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38684
hg19684
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226888
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594184
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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