A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599874



Internal ID20972945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14498085..14499148hg38UCSC Ensembl
chr21:15870406..15871469hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg381064
hg191064
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254126
Samples
Known GenesSAMSN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599874
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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