A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758019



Internal ID20533879
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 StatusM
Merged Variants
Supporting Variantsnssv16283497
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)nsv4758019
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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