A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258562



Internal ID20825602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207715158..207715439hg38UCSC Ensembl
chr2:208579882..208580163hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555191
Supporting Variants
Samples
Known GenesCCNYL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258562
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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