A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761353



Internal ID20537213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43227252..43389474hg38UCSC Ensembl
chr17:41379299..41466842hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38162223
hg1987544
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv45n199
Supporting Variantsnssv16264407
Samples
Known GenesLINC00854, LINC00910
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761353
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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