A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597689



Internal ID20970760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:24797411..25226815hg38UCSC Ensembl
chr21:26169725..26599129hg19UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg38429405
hg19429405
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252929
Samples
Known GenesLOC339622
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597689
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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