A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218854



Internal ID20785894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51628682..51629132hg38UCSC Ensembl
chr14:52095400..52095850hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38451
hg19451
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584185
Supporting Variants
Samples
Known GenesFRMD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218854
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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