A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258539



Internal ID20825579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207414026..207414525hg38UCSC Ensembl
chr2:208278750..208279249hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540910
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258539
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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