A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254067



Internal ID20821107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33741692..33742266hg38UCSC Ensembl
chr21:35113997..35114571hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38575
hg19575
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597772
Supporting Variants
Samples
Known GenesITSN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254067
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00029


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer