A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595966



Internal ID20969037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:31948277..31957510hg38UCSC Ensembl
chr21:33320589..33329822hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg389234
hg199234
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254014
Samples
Known GenesHUNK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595966
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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