A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552682



Internal ID20925808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:157884248..157885821hg38UCSC Ensembl
chr2:158740760..158742333hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg381574
hg191574
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255318
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552682
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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