A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558879



Internal ID20931950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110754507..110756300hg38UCSC Ensembl
chr6:111075710..111077503hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381794
hg191794
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267849
Samples
Known GenesCDK19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558879
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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