A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548451



Internal ID20921637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44663365..44664206hg38UCSC Ensembl
chr1:45129037..45129878hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38842
hg19842
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251846
Samples
Known GenesTMEM53
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548451
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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