A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595838



Internal ID20968909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:31727255..31727627hg38UCSC Ensembl
chr21:33099568..33099940hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4588n223
Supporting Variantsnssv18254000
Samples
Known GenesSCAF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595838
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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