A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596363



Internal ID20969434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29568978..29570449hg38UCSC Ensembl
chr19:30059885..30061356hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381472
hg191472
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245858
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596363
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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