A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219099



Internal ID20786139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20694430..20695141hg38UCSC Ensembl
chr14:21162589..21163300hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38712
hg19712
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590929
Supporting Variants
Samples
Known GenesRNASE4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219099
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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