A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248421



Internal ID20815461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40486215..40486514hg38UCSC Ensembl
chr19:40992122..40992421hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596238
Supporting Variants
Samples
Known GenesSPTBN4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248421
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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