A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596795



Internal ID20969866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15086053..15086492hg38UCSC Ensembl
chr19:15196864..15197303hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38440
hg19440
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245780
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596795
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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