A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543511



Internal ID20916757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:166865521..166866758hg38UCSC Ensembl
chr1:166834758..166835995hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg381238
hg191238
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248023
Samples
Known GenesTADA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543511
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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