A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553282



Internal ID20926391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28753826..28754264hg38UCSC Ensembl
chr1:29080338..29080776hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38439
hg19439
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252327
Samples
Known GenesYTHDF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553282
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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