A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283497



Internal ID20492715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:22253871..27921243hg38UCSC Ensembl
chr21:23626191..29293562hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg385667373
hg195667372
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758019
Supporting Variants
Samples
Known GenesADAMTS1, ADAMTS5, APP, ATP5J, CYYR1, D21S2088E, GABPA, JAM2, LINC00113, LINC00158, LINC00515, LOC339622, MIR155, MIR155HG, MIR4759, MIR5009, MRPL39
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283497
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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