A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220209



Internal ID20787249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:29404712..29405185hg38UCSC Ensembl
chr14:29873918..29874391hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579222
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220209
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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