A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583546



Internal ID20956617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:105350509..106541811hg38UCSC Ensembl
chr11:105221236..106412538hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381191303
hg191191303
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231292
Samples
Known GenesAASDHPPT, GRIA4, KBTBD3, MSANTD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583546
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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