A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255835



Internal ID20822876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165653778..165654704hg38UCSC Ensembl
chr2:166510288..166511214hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38927
hg19927
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550881
Supporting Variants
Samples
Known GenesCSRNP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255835
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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