A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555692



Internal ID20928763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112084907..112090583hg38UCSC Ensembl
chr6:112406110..112411786hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385677
hg195677
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268507
Samples
Known GenesFAM229B, TUBE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555692
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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