A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258611



Internal ID20825651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:210191150..210192351hg38UCSC Ensembl
chr2:211055874..211057075hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540308
Supporting Variants
Samples
Known GenesACADL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258611
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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