A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246273



Internal ID20813313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40772663..40773484hg38UCSC Ensembl
chr19:41278568..41279389hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38822
hg19822
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598743
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246273
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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