A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598389



Internal ID20971460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29278260..29278893hg38UCSC Ensembl
chr21:30650581..30651214hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38634
hg19634
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253031
Samples
Known GenesLINC00189
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598389
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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