A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590959



Internal ID20964030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16856160..16860780hg38UCSC Ensembl
chr11:16877707..16882327hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg384621
hg194621
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236550
Samples
Known GenesPLEKHA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590959
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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