A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578679



Internal ID20951750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83075436..83076721hg38UCSC Ensembl
chr11:82786478..82787763hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381286
hg191286
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1241n223
Supporting Variantsnssv18219699
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578679
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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