A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592801



Internal ID20965872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83075374..83076664hg38UCSC Ensembl
chr11:82786416..82787706hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381291
hg191291
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1241n223
Supporting Variantsnssv18219571
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592801
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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