A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580487



Internal ID20953558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86964295..86967171hg38UCSC Ensembl
chr11:86675337..86678213hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg382877
hg192877
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224245
Samples
Known GenesLOC100506368
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580487
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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