A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588299



Internal ID20961370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32202205..32202791hg38UCSC Ensembl
chr11:32223751..32224337hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38587
hg19587
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227406
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588299
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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