A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538924



Internal ID20912231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:224732676..224733265hg38UCSC Ensembl
chr2:225597393..225597982hg19UCSC Ensembl
Cytoband2q36.2
Allele length
AssemblyAllele length
hg38590
hg19590
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257151
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538924
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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