A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259295



Internal ID20826335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216085698..216086144hg38UCSC Ensembl
chr2:216950421..216950867hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553172
Supporting Variants
Samples
Known GenesTMEM169
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259295
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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