A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259687



Internal ID20826727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136864315..136865118hg38UCSC Ensembl
chr3:136583157..136583960hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38804
hg19804
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570805
Supporting Variants
Samples
Known GenesNCK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259687
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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