A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592685



Internal ID20965756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72520274..72520398hg38UCSC Ensembl
chr11:72231318..72231442hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217273
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592685
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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