A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237406



Internal ID20804446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65019045..65020427hg38UCSC Ensembl
chr14:65485763..65487145hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg381383
hg191383
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583551
Supporting Variants
Samples
Known GenesCHURC1-FNTB, FNTB, MAX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237406
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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