A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259614



Internal ID20826654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129175052..129175579hg38UCSC Ensembl
chr3:128893895..128894422hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38528
hg19528
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559324
Supporting Variants
Samples
Known GenesCNBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259614
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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