A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596452



Internal ID20969523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:31721846..31722713hg38UCSC Ensembl
chr21:33094159..33095026hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38868
hg19868
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253997
Samples
Known GenesSCAF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596452
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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