A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259401



Internal ID20826441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:222156178..222156912hg38UCSC Ensembl
chr2:223020897..223021631hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg38735
hg19735
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548905
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259401
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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