A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238354



Internal ID20805394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93205509..93206129hg38UCSC Ensembl
chr14:93671854..93672474hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38621
hg19621
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592124
Supporting Variants
Samples
Known GenesC14orf142
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238354
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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