A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545743



Internal ID20918969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113787654..113789652hg38UCSC Ensembl
chr2:114545231..114547229hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg381999
hg191999
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4086n223
Supporting Variantsnssv18256549
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545743
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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