A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545722



Internal ID20918947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235106781..235114993hg38UCSC Ensembl
chr1:235270096..235278308hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg388213
hg198213
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250681
Samples
Known GenesTOMM20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545722
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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