A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557983



Internal ID20931054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:54381604..54387211hg38UCSC Ensembl
chr6:54246402..54252009hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg385608
hg195608
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270952
Samples
Known GenesTINAG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557983
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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