A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237753



Internal ID20804793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:53124130..53125932hg38UCSC Ensembl
chr14:53590848..53592650hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg381803
hg191803
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586925
Supporting Variants
Samples
Known GenesDDHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237753
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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