A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256367



Internal ID20823407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:200993890..200994434hg38UCSC Ensembl
chr2:201858613..201859157hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38545
hg19545
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555039
Supporting Variants
Samples
Known GenesFAM126B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256367
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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