A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271053



Internal ID20838093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105055514..105056619hg38UCSC Ensembl
chr6:105503389..105504494hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381106
hg191106
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569169
Supporting Variants
Samples
Known GenesLIN28B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271053
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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