A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254767



Internal ID20821807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39457655..39458633hg38UCSC Ensembl
chr21:40829581..40830559hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38979
hg19979
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596939
Supporting Variants
Samples
Known GenesSH3BGR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254767
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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