A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536693



Internal ID20910038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151554690..151555498hg38UCSC Ensembl
chr1:151527166..151527974hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38809
hg19809
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248154
Samples
Known GenesTUFT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536693
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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