A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257250



Internal ID20824290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:228755053..228755240hg38UCSC Ensembl
chr2:229619769..229619956hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540723
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257250
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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