A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283313



Internal ID20492531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43323821..43386526hg38UCSC Ensembl
chr17:41401189..41463894hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3862706
hg1962706
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756332
Supporting Variants
Samples
Known GenesLINC00910
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283313
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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