A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238694



Internal ID20805734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73855644..73855921hg38UCSC Ensembl
chr14:74322347..74322624hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594970
Supporting Variants
Samples
Known GenesPTGR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238694
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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