A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599786



Internal ID20972857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9241028..9241732hg38UCSC Ensembl
chr19:9351704..9352408hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38705
hg19705
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246538
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599786
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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