A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535933



Internal ID20909286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151554795..151555327hg38UCSC Ensembl
chr1:151527271..151527803hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248155
Samples
Known GenesTUFT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535933
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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