A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230621



Internal ID20797661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:31040542..31972775hg38UCSC Ensembl
chr14:31509748..32441981hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38932234
hg19932234
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576555
Supporting Variants
Samples
Known GenesAP4S1, DTD2, GPR33, HEATR5A, HECTD1, NUBPL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230621
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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