A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245865



Internal ID20812905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29987885..29989408hg38UCSC Ensembl
chr19:30478792..30480315hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381524
hg191524
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600067
Supporting Variants
Samples
Known GenesURI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245865
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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