A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598065



Internal ID20971136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43012374..43014345hg38UCSC Ensembl
chr21:44432484..44434455hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381972
hg191972
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254482
Samples
Known GenesPKNOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598065
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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