A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233132



Internal ID20800172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32470130..32471302hg38UCSC Ensembl
chr14:32939336..32940508hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg381173
hg191173
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576173
Supporting Variants
Samples
Known GenesAKAP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233132
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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