A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259799



Internal ID20826839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15848652..15848785hg38UCSC Ensembl
chr3:15890159..15890292hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542798
Supporting Variants
Samples
Known GenesANKRD28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259799
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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