A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556867



Internal ID20929938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138694764..138696112hg38UCSC Ensembl
chr6:139015901..139017249hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg381349
hg191349
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272467
Samples
Known GenesFLJ46906
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556867
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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