A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588879



Internal ID20961950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:115565375..115565794hg38UCSC Ensembl
chr11:115436093..115436512hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38420
hg19420
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235673
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588879
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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