A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254714



Internal ID20821754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36982983..36983444hg38UCSC Ensembl
chr21:38355283..38355744hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600069
Supporting Variants
Samples
Known GenesHLCS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254714
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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