A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596091



Internal ID20969162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26155251..26157110hg38UCSC Ensembl
chr21:27527569..27529428hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg381860
hg191860
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252967
Samples
Known GenesAPP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596091
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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