A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548253



Internal ID20921449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:224335887..224336515hg38UCSC Ensembl
chr1:224523589..224524217hg19UCSC Ensembl
Cytoband1q42.11
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv544n223
Supporting Variantsnssv18249373
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548253
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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