A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220562



Internal ID20787602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39150539..39151291hg38UCSC Ensembl
chr14:39619743..39620495hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588706
Supporting Variants
Samples
Known GenesTRAPPC6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220562
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00021


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