A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261413



Internal ID20828453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52740608..52745218hg38UCSC Ensembl
chr3:52774624..52779234hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg384611
hg194611
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535618
Supporting Variants
Samples
Known GenesNEK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261413
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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