A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536267



Internal ID20909620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16343427..16344165hg38UCSC Ensembl
chr1:16669922..16670660hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38739
hg19739
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247970
Samples
Known GenesFBXO42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536267
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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