A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246579



Internal ID20813619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34217250..34217561hg38UCSC Ensembl
chr19:34708155..34708466hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599463
Supporting Variants
Samples
Known GenesLSM14A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246579
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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