A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248327



Internal ID20815367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37499801..37500981hg38UCSC Ensembl
chr19:37990703..37991883hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381181
hg191181
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596726
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248327
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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