A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248197



Internal ID20815237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19777014..19777348hg38UCSC Ensembl
chr1:20103507..20103841hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543186
Supporting Variants
Samples
Known GenesTMCO4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248197
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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