A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598978



Internal ID20972049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2879354..2880043hg38UCSC Ensembl
chr19:2879352..2880041hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38690
hg19690
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245852
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598978
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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