A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577262



Internal ID20950333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60067752..60068447hg38UCSC Ensembl
chr11:59835225..59835920hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38696
hg19696
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1200n223
Supporting Variantsnssv18236330
Samples
Known GenesMS4A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577262
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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