A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222572



Internal ID20789612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:30334989..30335607hg38UCSC Ensembl
chr14:30804195..30804813hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38619
hg19619
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581625
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222572
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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