A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759053



Internal ID20534913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43304234..43388636hg38UCSC Ensembl
chr17:41381583..41466004hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3884403
hg1984422
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv45n199
Supporting Variantsnssv16272797
Samples
Known GenesLINC00910
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759053
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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