A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588660



Internal ID20961731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77564660..77565754hg38UCSC Ensembl
chr11:77275705..77276799hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381095
hg191095
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222033
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588660
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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