A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110527



Internal ID22019760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57044918..57066117hg38UCSC Ensembl
chr17:55122279..55143478hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3821200
hg1921200
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630531
Samples
Known GenesRNF126P1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110527
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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