A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545886



Internal ID20919110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:113722708..113723194hg38UCSC Ensembl
chr1:114265330..114265816hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38487
hg19487
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249222
Samples
Known GenesPHTF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545886
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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