A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577259



Internal ID20950330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46224110..46224503hg38UCSC Ensembl
chr11:46245661..46246054hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38394
hg19394
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224377
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577259
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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