A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579628



Internal ID20952699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:109538234..109612581hg38UCSC Ensembl
chr11:109408960..109483307hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3874348
hg1974348
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223452
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579628
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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