A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546481



Internal ID20875415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:189413986..189414741hg38UCSC Ensembl
chr2:190278712..190279467hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg38756
hg19756
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4227n223
Supporting Variantsnssv18256959
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546481
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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