A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221916



Internal ID20788956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51824223..51825238hg38UCSC Ensembl
chr14:52290941..52291956hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg381016
hg191016
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579964
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221916
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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