A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260288



Internal ID20827328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134227676..134228297hg38UCSC Ensembl
chr3:133946520..133947141hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38622
hg19622
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571010
Supporting Variants
Samples
Known GenesRYK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260288
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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