A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3545874



Internal ID22414877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26000477..26003856hg38UCSC Ensembl
chr21:27372792..27376171hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg383380
hg193380
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14461752, nssv14458067, nssv14459400, nssv14457278, nssv14462953, nssv14461256
SamplesHG00512, NA19239, HG00732, NA19240, HG00733, HG00513
Known GenesAPP
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3545874
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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