A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225033



Internal ID20792073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52457740..52459920hg38UCSC Ensembl
chr14:52924458..52926638hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg382181
hg192181
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594691
Supporting Variants
Samples
Known GenesTXNDC16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225033
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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