A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254024



Internal ID20821064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32671778..32672631hg38UCSC Ensembl
chr21:34044088..34044941hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38854
hg19854
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599407
Supporting Variants
Samples
Known GenesSYNJ1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254024
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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