A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249097



Internal ID20816137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57562832..57563309hg38UCSC Ensembl
chr19:58074200..58074677hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596854
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249097
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00021


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